Name: rs148821778
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs148821778

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:64677439-64677464 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₇ / del(A)₁₆ / del(A)₁₅ / d…
del(A)₁₇ / del(A)₁₆ / del(A)₁₅ / del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.1214 (468/3854, ALSPAC)
del(A)₁₇=0.000 (0/954, ALFA)
del(A)₁₆=0.000 (0/954, ALFA) (+ 18 more)
del(A)₁₅=0.000 (0/954, ALFA)
del(A)₁₄=0.000 (0/954, ALFA)
del(A)₁₃=0.000 (0/954, ALFA)
del(A)₁₂=0.000 (0/954, ALFA)
del(A)₁₁=0.000 (0/954, ALFA)
del(A)₁₀=0.000 (0/954, ALFA)
del(A)₉=0.000 (0/954, ALFA)
del(A)₈=0.000 (0/954, ALFA)
del(A)₇=0.000 (0/954, ALFA)
del(A)₆=0.000 (0/954, ALFA)
del(A)₅=0.000 (0/954, ALFA)
del(A)₄=0.000 (0/954, ALFA)
delAAA=0.000 (0/954, ALFA)
delAA=0.000 (0/954, ALFA)
delA=0.000 (0/954, ALFA)
dupA=0.000 (0/954, ALFA)
dupAA=0.000 (0/954, ALFA)
dupAAA=0.000 (0/954, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP7B1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	954	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
European	Sub	430	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	410	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	22	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	388	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 2	Sub	44	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
South Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	28	AAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₂₆=0.8786	del(A)₁₁=0.1214
Allele Frequency Aggregator	Total	Global	954	(A)₂₆=1.000	del(A)₁₇=0.000, del(A)₁₆=0.000, del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	European	Sub	430	(A)₂₆=1.000	del(A)₁₇=0.000, del(A)₁₆=0.000, del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	African	Sub	410	(A)₂₆=1.000	del(A)₁₇=0.000, del(A)₁₆=0.000, del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	44	(A)₂₆=1.00	del(A)₁₇=0.00, del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Other	Sub	28	(A)₂₆=1.00	del(A)₁₇=0.00, del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	24	(A)₂₆=1.00	del(A)₁₇=0.00, del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(A)₂₆=1.0	del(A)₁₇=0.0, del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₂₆=1.0	del(A)₁₇=0.0, del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 8	NC_000008.11:g.64677448_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677449_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677450_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677451_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677452_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677453_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677454_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677455_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677456_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677457_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677458_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677459_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677460_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677461_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677462_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677463_64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677464del
GRCh38.p14 chr 8	NC_000008.11:g.64677464dup
GRCh38.p14 chr 8	NC_000008.11:g.64677463_64677464dup
GRCh38.p14 chr 8	NC_000008.11:g.64677462_64677464dup
GRCh37.p13 chr 8	NC_000008.10:g.65590005_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590006_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590007_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590008_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590009_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590010_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590011_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590012_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590013_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590014_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590015_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590016_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590017_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590018_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590019_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590020_65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590021del
GRCh37.p13 chr 8	NC_000008.10:g.65590021dup
GRCh37.p13 chr 8	NC_000008.10:g.65590020_65590021dup
GRCh37.p13 chr 8	NC_000008.10:g.65590019_65590021dup
CYP7B1 RefSeqGene	NG_008338.2:g.126337_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126338_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126339_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126340_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126341_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126342_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126343_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126344_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126345_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126346_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126347_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126348_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126349_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126350_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126351_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126352_126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126353del
CYP7B1 RefSeqGene	NG_008338.2:g.126353dup
CYP7B1 RefSeqGene	NG_008338.2:g.126352_126353dup
CYP7B1 RefSeqGene	NG_008338.2:g.126351_126353dup

Gene: CYP7B1, cytochrome P450 family 7 subfamily B member 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CYP7B1 transcript variant 2	NM_001324112.2:c.123-5291… NM_001324112.2:c.123-52916_123-52900del	N/A	Intron Variant
CYP7B1 transcript variant 1	NM_004820.5:c.123-52916_1… NM_004820.5:c.123-52916_123-52900del	N/A	Intron Variant
CYP7B1 transcript variant X1	XM_017014002.2:c.188+1447… XM_017014002.2:c.188+14471_188+14487del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₂₆=	del(A)₁₇	del(A)₁₆	del(A)₁₅	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 8	NC_000008.11:g.64677439_64677464=	NC_000008.11:g.64677448_64677464del	NC_000008.11:g.64677449_64677464del	NC_000008.11:g.64677450_64677464del	NC_000008.11:g.64677451_64677464del	NC_000008.11:g.64677452_64677464del	NC_000008.11:g.64677453_64677464del	NC_000008.11:g.64677454_64677464del	NC_000008.11:g.64677455_64677464del	NC_000008.11:g.64677456_64677464del	NC_000008.11:g.64677457_64677464del	NC_000008.11:g.64677458_64677464del	NC_000008.11:g.64677459_64677464del	NC_000008.11:g.64677460_64677464del	NC_000008.11:g.64677461_64677464del	NC_000008.11:g.64677462_64677464del	NC_000008.11:g.64677463_64677464del	NC_000008.11:g.64677464del	NC_000008.11:g.64677464dup	NC_000008.11:g.64677463_64677464dup	NC_000008.11:g.64677462_64677464dup
GRCh37.p13 chr 8	NC_000008.10:g.65589996_65590021=	NC_000008.10:g.65590005_65590021del	NC_000008.10:g.65590006_65590021del	NC_000008.10:g.65590007_65590021del	NC_000008.10:g.65590008_65590021del	NC_000008.10:g.65590009_65590021del	NC_000008.10:g.65590010_65590021del	NC_000008.10:g.65590011_65590021del	NC_000008.10:g.65590012_65590021del	NC_000008.10:g.65590013_65590021del	NC_000008.10:g.65590014_65590021del	NC_000008.10:g.65590015_65590021del	NC_000008.10:g.65590016_65590021del	NC_000008.10:g.65590017_65590021del	NC_000008.10:g.65590018_65590021del	NC_000008.10:g.65590019_65590021del	NC_000008.10:g.65590020_65590021del	NC_000008.10:g.65590021del	NC_000008.10:g.65590021dup	NC_000008.10:g.65590020_65590021dup	NC_000008.10:g.65590019_65590021dup
CYP7B1 RefSeqGene	NG_008338.2:g.126328_126353=	NG_008338.2:g.126337_126353del	NG_008338.2:g.126338_126353del	NG_008338.2:g.126339_126353del	NG_008338.2:g.126340_126353del	NG_008338.2:g.126341_126353del	NG_008338.2:g.126342_126353del	NG_008338.2:g.126343_126353del	NG_008338.2:g.126344_126353del	NG_008338.2:g.126345_126353del	NG_008338.2:g.126346_126353del	NG_008338.2:g.126347_126353del	NG_008338.2:g.126348_126353del	NG_008338.2:g.126349_126353del	NG_008338.2:g.126350_126353del	NG_008338.2:g.126351_126353del	NG_008338.2:g.126352_126353del	NG_008338.2:g.126353del	NG_008338.2:g.126353dup	NG_008338.2:g.126352_126353dup	NG_008338.2:g.126351_126353dup
CYP7B1 transcript variant 2	NM_001324112.2:c.123-52900=	NM_001324112.2:c.123-52916_123-52900del	NM_001324112.2:c.123-52915_123-52900del	NM_001324112.2:c.123-52914_123-52900del	NM_001324112.2:c.123-52913_123-52900del	NM_001324112.2:c.123-52912_123-52900del	NM_001324112.2:c.123-52911_123-52900del	NM_001324112.2:c.123-52910_123-52900del	NM_001324112.2:c.123-52909_123-52900del	NM_001324112.2:c.123-52908_123-52900del	NM_001324112.2:c.123-52907_123-52900del	NM_001324112.2:c.123-52906_123-52900del	NM_001324112.2:c.123-52905_123-52900del	NM_001324112.2:c.123-52904_123-52900del	NM_001324112.2:c.123-52903_123-52900del	NM_001324112.2:c.123-52902_123-52900del	NM_001324112.2:c.123-52901_123-52900del	NM_001324112.2:c.123-52900del	NM_001324112.2:c.123-52900dup	NM_001324112.2:c.123-52901_123-52900dup	NM_001324112.2:c.123-52902_123-52900dup
CYP7B1 transcript	NM_004820.3:c.123-52900=	NM_004820.3:c.123-52916_123-52900del	NM_004820.3:c.123-52915_123-52900del	NM_004820.3:c.123-52914_123-52900del	NM_004820.3:c.123-52913_123-52900del	NM_004820.3:c.123-52912_123-52900del	NM_004820.3:c.123-52911_123-52900del	NM_004820.3:c.123-52910_123-52900del	NM_004820.3:c.123-52909_123-52900del	NM_004820.3:c.123-52908_123-52900del	NM_004820.3:c.123-52907_123-52900del	NM_004820.3:c.123-52906_123-52900del	NM_004820.3:c.123-52905_123-52900del	NM_004820.3:c.123-52904_123-52900del	NM_004820.3:c.123-52903_123-52900del	NM_004820.3:c.123-52902_123-52900del	NM_004820.3:c.123-52901_123-52900del	NM_004820.3:c.123-52900del	NM_004820.3:c.123-52900dup	NM_004820.3:c.123-52901_123-52900dup	NM_004820.3:c.123-52902_123-52900dup
CYP7B1 transcript variant 1	NM_004820.5:c.123-52900=	NM_004820.5:c.123-52916_123-52900del	NM_004820.5:c.123-52915_123-52900del	NM_004820.5:c.123-52914_123-52900del	NM_004820.5:c.123-52913_123-52900del	NM_004820.5:c.123-52912_123-52900del	NM_004820.5:c.123-52911_123-52900del	NM_004820.5:c.123-52910_123-52900del	NM_004820.5:c.123-52909_123-52900del	NM_004820.5:c.123-52908_123-52900del	NM_004820.5:c.123-52907_123-52900del	NM_004820.5:c.123-52906_123-52900del	NM_004820.5:c.123-52905_123-52900del	NM_004820.5:c.123-52904_123-52900del	NM_004820.5:c.123-52903_123-52900del	NM_004820.5:c.123-52902_123-52900del	NM_004820.5:c.123-52901_123-52900del	NM_004820.5:c.123-52900del	NM_004820.5:c.123-52900dup	NM_004820.5:c.123-52901_123-52900dup	NM_004820.5:c.123-52902_123-52900dup
CYP7B1 transcript variant X1	XM_017014002.2:c.188+14487=	XM_017014002.2:c.188+14471_188+14487del	XM_017014002.2:c.188+14472_188+14487del	XM_017014002.2:c.188+14473_188+14487del	XM_017014002.2:c.188+14474_188+14487del	XM_017014002.2:c.188+14475_188+14487del	XM_017014002.2:c.188+14476_188+14487del	XM_017014002.2:c.188+14477_188+14487del	XM_017014002.2:c.188+14478_188+14487del	XM_017014002.2:c.188+14479_188+14487del	XM_017014002.2:c.188+14480_188+14487del	XM_017014002.2:c.188+14481_188+14487del	XM_017014002.2:c.188+14482_188+14487del	XM_017014002.2:c.188+14483_188+14487del	XM_017014002.2:c.188+14484_188+14487del	XM_017014002.2:c.188+14485_188+14487del	XM_017014002.2:c.188+14486_188+14487del	XM_017014002.2:c.188+14487del	XM_017014002.2:c.188+14487dup	XM_017014002.2:c.188+14486_188+14487dup	XM_017014002.2:c.188+14485_188+14487dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

64 SubSNP, 38 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95494072	Mar 15, 2016 (147)
2	GMI	ss288911995	May 04, 2012 (137)
3	PJP	ss295384180	May 09, 2011 (134)
4	EVA_UK10K_ALSPAC	ss1706082872	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1706082912	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1710384326	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1710384327	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1710384349	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710384351	Apr 01, 2015 (144)
10	SWEGEN	ss3003313305	Nov 08, 2017 (151)
11	MCHAISSO	ss3065189952	Nov 08, 2017 (151)
12	MCHAISSO	ss3066205832	Nov 08, 2017 (151)
13	URBANLAB	ss3648930965	Oct 12, 2018 (152)
14	EVA_DECODE	ss3722175499	Jul 13, 2019 (153)
15	EVA_DECODE	ss3722175500	Jul 13, 2019 (153)
16	EVA_DECODE	ss3722175501	Jul 13, 2019 (153)
17	EVA_DECODE	ss3722175502	Jul 13, 2019 (153)
18	EVA_DECODE	ss3722175503	Jul 13, 2019 (153)
19	EVA_DECODE	ss3722175504	Jul 13, 2019 (153)
20	ACPOP	ss3735733223	Jul 13, 2019 (153)
21	ACPOP	ss3735733224	Jul 13, 2019 (153)
22	ACPOP	ss3735733225	Jul 13, 2019 (153)
23	EVA	ss3831203783	Apr 26, 2020 (154)
24	GNOMAD	ss4185840982	Apr 26, 2021 (155)
25	GNOMAD	ss4185840983	Apr 26, 2021 (155)
26	GNOMAD	ss4185840984	Apr 26, 2021 (155)
27	GNOMAD	ss4185840985	Apr 26, 2021 (155)
28	GNOMAD	ss4185840986	Apr 26, 2021 (155)
29	GNOMAD	ss4185840987	Apr 26, 2021 (155)
30	GNOMAD	ss4185840988	Apr 26, 2021 (155)
31	GNOMAD	ss4185840989	Apr 26, 2021 (155)
32	GNOMAD	ss4185840990	Apr 26, 2021 (155)
33	GNOMAD	ss4185840991	Apr 26, 2021 (155)
34	GNOMAD	ss4185840992	Apr 26, 2021 (155)
35	GNOMAD	ss4185840993	Apr 26, 2021 (155)
36	GNOMAD	ss4185840994	Apr 26, 2021 (155)
37	GNOMAD	ss4185840995	Apr 26, 2021 (155)
38	GNOMAD	ss4185840996	Apr 26, 2021 (155)
39	GNOMAD	ss4185840997	Apr 26, 2021 (155)
40	GNOMAD	ss4185840998	Apr 26, 2021 (155)
41	GNOMAD	ss4185840999	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5189078547	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5189078548	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5189078549	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5189078550	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5189078551	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5189078552	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5277429970	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5277429971	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5277429972	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5277429973	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5277429974	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5473967363	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5473967364	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5473967365	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5473967366	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5473967367	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5473967368	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5731250154	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5731250155	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5731250156	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5731250157	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5731250158	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5731250159	Oct 16, 2022 (156)
65	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 65589996	Oct 12, 2018 (152)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 298453284 (NC_000008.11:64677438::A 1350/80452) Row 298453285 (NC_000008.11:64677438::AA 23/80492) Row 298453286 (NC_000008.11:64677438::AAA 6/80500)...	-	Apr 26, 2021 (155)
84	Northern Sweden Submission ignored due to conflicting rows: Row 9018088 (NC_000008.10:65589995:AAAA: 11/520) Row 9018089 (NC_000008.10:65589995:AAA: 40/520) Row 9018090 (NC_000008.10:65589995:AAAAAAAAAAA: 15/520)	-	Jul 13, 2019 (153)
85	Northern Sweden Submission ignored due to conflicting rows: Row 9018088 (NC_000008.10:65589995:AAAA: 11/520) Row 9018089 (NC_000008.10:65589995:AAA: 40/520) Row 9018090 (NC_000008.10:65589995:AAAAAAAAAAA: 15/520)	-	Jul 13, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 9018088 (NC_000008.10:65589995:AAAA: 11/520) Row 9018089 (NC_000008.10:65589995:AAA: 40/520) Row 9018090 (NC_000008.10:65589995:AAAAAAAAAAA: 15/520)	-	Jul 13, 2019 (153)
87	8.3KJPN Submission ignored due to conflicting rows: Row 47047854 (NC_000008.10:65589995:AAAAAAA: 688/16554) Row 47047855 (NC_000008.10:65589995:AAAAAA: 2154/16554) Row 47047856 (NC_000008.10:65589995:AAA: 4209/16554)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 47047854 (NC_000008.10:65589995:AAAAAAA: 688/16554) Row 47047855 (NC_000008.10:65589995:AAAAAA: 2154/16554) Row 47047856 (NC_000008.10:65589995:AAA: 4209/16554)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 47047854 (NC_000008.10:65589995:AAAAAAA: 688/16554) Row 47047855 (NC_000008.10:65589995:AAAAAA: 2154/16554) Row 47047856 (NC_000008.10:65589995:AAA: 4209/16554)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 47047854 (NC_000008.10:65589995:AAAAAAA: 688/16554) Row 47047855 (NC_000008.10:65589995:AAAAAA: 2154/16554) Row 47047856 (NC_000008.10:65589995:AAA: 4209/16554)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 47047854 (NC_000008.10:65589995:AAAAAAA: 688/16554) Row 47047855 (NC_000008.10:65589995:AAAAAA: 2154/16554) Row 47047856 (NC_000008.10:65589995:AAA: 4209/16554)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 47047854 (NC_000008.10:65589995:AAAAAAA: 688/16554) Row 47047855 (NC_000008.10:65589995:AAAAAA: 2154/16554) Row 47047856 (NC_000008.10:65589995:AAA: 4209/16554)...	-	Apr 26, 2021 (155)
93	14KJPN Submission ignored due to conflicting rows: Row 65087258 (NC_000008.11:64677438:AAAAAA: 4271/28054) Row 65087259 (NC_000008.11:64677438:AAA: 8569/28054) Row 65087260 (NC_000008.11:64677438:AAAAAAA: 1343/28054)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 65087258 (NC_000008.11:64677438:AAAAAA: 4271/28054) Row 65087259 (NC_000008.11:64677438:AAA: 8569/28054) Row 65087260 (NC_000008.11:64677438:AAAAAAA: 1343/28054)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 65087258 (NC_000008.11:64677438:AAAAAA: 4271/28054) Row 65087259 (NC_000008.11:64677438:AAA: 8569/28054) Row 65087260 (NC_000008.11:64677438:AAAAAAA: 1343/28054)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 65087258 (NC_000008.11:64677438:AAAAAA: 4271/28054) Row 65087259 (NC_000008.11:64677438:AAA: 8569/28054) Row 65087260 (NC_000008.11:64677438:AAAAAAA: 1343/28054)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 65087258 (NC_000008.11:64677438:AAAAAA: 4271/28054) Row 65087259 (NC_000008.11:64677438:AAA: 8569/28054) Row 65087260 (NC_000008.11:64677438:AAAAAAA: 1343/28054)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 65087258 (NC_000008.11:64677438:AAAAAA: 4271/28054) Row 65087259 (NC_000008.11:64677438:AAA: 8569/28054) Row 65087260 (NC_000008.11:64677438:AAAAAAA: 1343/28054)...	-	Oct 16, 2022 (156)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23539132 (NC_000008.10:65590001:AAAAA: 1369/3708) Row 23539133 (NC_000008.10:65590002:AAAA: 1807/3708) Row 23539134 (NC_000008.10:65589995:AAAAAAAAAAA: 405/3708)	-	Apr 26, 2020 (154)
100	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23539132 (NC_000008.10:65590001:AAAAA: 1369/3708) Row 23539133 (NC_000008.10:65590002:AAAA: 1807/3708) Row 23539134 (NC_000008.10:65589995:AAAAAAAAAAA: 405/3708)	-	Apr 26, 2020 (154)
101	UK 10K study - Twins	-	Oct 12, 2018 (152)
102	ALFA	NC_000008.11 - 64677439	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs71260894	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4185840999	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss5189078550	NC_000008.10:65589995:AAAAAAAAAAAA… NC_000008.10:65589995:AAAAAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4185840998, ss5731250158	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4185840997	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4185840996	NC_000008.11:64677438:AAAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
23539134, ss1706082872, ss1706082912, ss3003313305, ss3735733225, ss3831203783	NC_000008.10:65589995:AAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3066205832, ss3722175504, ss4185840995, ss5277429971, ss5473967363	NC_000008.11:64677438:AAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4185840994	NC_000008.11:64677438:AAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4185840993	NC_000008.11:64677438:AAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss288911995	NC_000008.9:65752549:AAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4185840992	NC_000008.11:64677438:AAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5189078547	NC_000008.10:65589995:AAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4185840991, ss5731250156	NC_000008.11:64677438:AAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5189078548	NC_000008.10:65589995:AAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4185840990, ss5277429970, ss5473967367, ss5731250154	NC_000008.11:64677438:AAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3722175503	NC_000008.11:64677443:AAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss1710384326, ss1710384349	NC_000008.10:65590001:AAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3648930965, ss4185840989, ss5473967366	NC_000008.11:64677438:AAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3722175502	NC_000008.11:64677444:AAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3735733223, ss5189078551	NC_000008.10:65589995:AAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss1710384327, ss1710384351	NC_000008.10:65590002:AAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3065189952, ss4185840988, ss5277429974, ss5473967364, ss5731250157	NC_000008.11:64677438:AAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3722175501	NC_000008.11:64677445:AAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss295384180	NC_000008.9:65752549:AAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3735733224, ss5189078549	NC_000008.10:65589995:AAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4185840987, ss5473967365, ss5731250155	NC_000008.11:64677438:AAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3722175500	NC_000008.11:64677446:AAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95494072	NT_008183.19:17454419:AAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4185840986, ss5277429972, ss5473967368	NC_000008.11:64677438:AA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3722175499	NC_000008.11:64677447:AA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5189078552	NC_000008.10:65589995:A:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4185840985, ss5277429973, ss5731250159	NC_000008.11:64677438:A:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4185840982	NC_000008.11:64677438::A	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4185840983	NC_000008.11:64677438::AA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4185840984	NC_000008.11:64677438::AAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12374977534	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3564375173	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAA:	NC_000008.11:64677438:AAAAAAAAAAAA… NC_000008.11:64677438:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs148821778

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs148821778