Name: rs71154831
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.

rs71154831

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:207642011-207642034 (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(T)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₇ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / ins(T)₄₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1621 (1220/7526, ALFA)
del(T)₁₁=0.4509 (2258/5008, 1000G)
(T)₂₄=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CR1 : 500B Downstream 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	Alt HMOZ	HTRZ	HWEP
Total	Global	7526	TTTTTTTTTTTTTTTTTTTTTTTT=0.8134	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0114, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTTTTT=0.1621, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0069, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0045, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.77843	0.093602	0.127969	32
European	Sub	6940	TTTTTTTTTTTTTTTTTTTTTTTT=0.7983	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0124, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTTTT=0.1752, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0075, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0049, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.759586	0.101643	0.138771	32
African	Sub	350	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	338	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	36	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	74	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	108	TTTTTTTTTTTTTTTTTTTTTTTT=0.963	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.037, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.944444	0.018519	0.037037	7

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
Allele Frequency Aggregator	Total	Global	7526	(T)₂₄=0.8134	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0114, delTT=0.0000, delT=0.0016, dupT=0.1621, dupTT=0.0069, dupTTT=0.0045, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	6940	(T)₂₄=0.7983	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0124, delTT=0.0000, delT=0.0017, dupT=0.1752, dupTT=0.0075, dupTTT=0.0049, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	350	(T)₂₄=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	108	(T)₂₄=0.963	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.037, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	74	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	36	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Asian	Sub	6	(T)₂₄=1.0	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0
1000Genomes	Global	Study-wide	5008	(T)₂₄=0.5491	del(T)₁₁=0.4509
1000Genomes	African	Sub	1322	(T)₂₄=0.2526	del(T)₁₁=0.7474
1000Genomes	East Asian	Sub	1008	(T)₂₄=0.5883	del(T)₁₁=0.4117
1000Genomes	Europe	Sub	1006	(T)₂₄=0.6501	del(T)₁₁=0.3499
1000Genomes	South Asian	Sub	978	(T)₂₄=0.680	del(T)₁₁=0.320
1000Genomes	American	Sub	694	(T)₂₄=0.726	del(T)₁₁=0.274
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.65

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 1	NC_000001.11:g.207642022_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642023_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642024_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642025_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642026_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642028_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642029_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642031_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642032_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642033_207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642034del
GRCh38.p14 chr 1	NC_000001.11:g.207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642033_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642032_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642031_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642030_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642029_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642028_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642027_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642026_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642025_207642034dup
GRCh38.p14 chr 1	NC_000001.11:g.207642034_207642035insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.207815367_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815368_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815369_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815370_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815371_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815373_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815374_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815376_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815377_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815378_207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815379del
GRCh37.p13 chr 1	NC_000001.10:g.207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815378_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815377_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815376_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815375_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815374_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815373_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815372_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815371_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815370_207815379dup
GRCh37.p13 chr 1	NC_000001.10:g.207815379_207815380insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150895_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150896_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150897_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150898_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150899_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150901_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150902_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150904_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150905_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150906_150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150907del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150906_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150905_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150904_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150903_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150902_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150901_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150900_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150899_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150898_150907dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150907_150908insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: CR1, complement C3b/C4b receptor 1 (Knops blood group) (plus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
CR1 transcript variant S	NM_000651.6:c.	N/A	Downstream Transcript 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	(T)₂₄=	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₇	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	ins(T)₄₄
GRCh38.p14 chr 1	NC_000001.11:g.207642011_207642034=	NC_000001.11:g.207642022_207642034del	NC_000001.11:g.207642023_207642034del	NC_000001.11:g.207642024_207642034del	NC_000001.11:g.207642025_207642034del	NC_000001.11:g.207642026_207642034del	NC_000001.11:g.207642028_207642034del	NC_000001.11:g.207642029_207642034del	NC_000001.11:g.207642031_207642034del	NC_000001.11:g.207642032_207642034del	NC_000001.11:g.207642033_207642034del	NC_000001.11:g.207642034del	NC_000001.11:g.207642034dup	NC_000001.11:g.207642033_207642034dup	NC_000001.11:g.207642032_207642034dup	NC_000001.11:g.207642031_207642034dup	NC_000001.11:g.207642030_207642034dup	NC_000001.11:g.207642029_207642034dup	NC_000001.11:g.207642028_207642034dup	NC_000001.11:g.207642027_207642034dup	NC_000001.11:g.207642026_207642034dup	NC_000001.11:g.207642025_207642034dup	NC_000001.11:g.207642034_207642035insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.207815356_207815379=	NC_000001.10:g.207815367_207815379del	NC_000001.10:g.207815368_207815379del	NC_000001.10:g.207815369_207815379del	NC_000001.10:g.207815370_207815379del	NC_000001.10:g.207815371_207815379del	NC_000001.10:g.207815373_207815379del	NC_000001.10:g.207815374_207815379del	NC_000001.10:g.207815376_207815379del	NC_000001.10:g.207815377_207815379del	NC_000001.10:g.207815378_207815379del	NC_000001.10:g.207815379del	NC_000001.10:g.207815379dup	NC_000001.10:g.207815378_207815379dup	NC_000001.10:g.207815377_207815379dup	NC_000001.10:g.207815376_207815379dup	NC_000001.10:g.207815375_207815379dup	NC_000001.10:g.207815374_207815379dup	NC_000001.10:g.207815373_207815379dup	NC_000001.10:g.207815372_207815379dup	NC_000001.10:g.207815371_207815379dup	NC_000001.10:g.207815370_207815379dup	NC_000001.10:g.207815379_207815380insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.150884_150907=	NG_007481.1:g.150895_150907del	NG_007481.1:g.150896_150907del	NG_007481.1:g.150897_150907del	NG_007481.1:g.150898_150907del	NG_007481.1:g.150899_150907del	NG_007481.1:g.150901_150907del	NG_007481.1:g.150902_150907del	NG_007481.1:g.150904_150907del	NG_007481.1:g.150905_150907del	NG_007481.1:g.150906_150907del	NG_007481.1:g.150907del	NG_007481.1:g.150907dup	NG_007481.1:g.150906_150907dup	NG_007481.1:g.150905_150907dup	NG_007481.1:g.150904_150907dup	NG_007481.1:g.150903_150907dup	NG_007481.1:g.150902_150907dup	NG_007481.1:g.150901_150907dup	NG_007481.1:g.150900_150907dup	NG_007481.1:g.150899_150907dup	NG_007481.1:g.150898_150907dup	NG_007481.1:g.150907_150908insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

47 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95253280	Feb 13, 2009 (130)
2	PJP	ss294622342	Oct 11, 2018 (152)
3	1000GENOMES	ss1367977084	Aug 21, 2014 (142)
4	EVA_GENOME_DK	ss1574085321	Apr 01, 2015 (144)
5	SWEGEN	ss2988344893	Nov 08, 2017 (151)
6	KHV_HUMAN_GENOMES	ss3800261349	Jul 12, 2019 (153)
7	EVA	ss3826610201	Apr 25, 2020 (154)
8	GNOMAD	ss4010205007	Apr 25, 2021 (155)
9	GNOMAD	ss4010205008	Apr 25, 2021 (155)
10	GNOMAD	ss4010205009	Apr 25, 2021 (155)
11	GNOMAD	ss4010205010	Apr 25, 2021 (155)
12	GNOMAD	ss4010205011	Apr 25, 2021 (155)
13	GNOMAD	ss4010205012	Apr 25, 2021 (155)
14	GNOMAD	ss4010205013	Apr 25, 2021 (155)
15	GNOMAD	ss4010205014	Apr 25, 2021 (155)
16	GNOMAD	ss4010205015	Apr 25, 2021 (155)
17	GNOMAD	ss4010205016	Apr 25, 2021 (155)
18	GNOMAD	ss4010205017	Apr 25, 2021 (155)
19	GNOMAD	ss4010205019	Apr 25, 2021 (155)
20	GNOMAD	ss4010205020	Apr 25, 2021 (155)
21	GNOMAD	ss4010205021	Apr 25, 2021 (155)
22	GNOMAD	ss4010205022	Apr 25, 2021 (155)
23	GNOMAD	ss4010205023	Apr 25, 2021 (155)
24	GNOMAD	ss4010205024	Apr 25, 2021 (155)
25	GNOMAD	ss4010205025	Apr 25, 2021 (155)
26	GNOMAD	ss4010205026	Apr 25, 2021 (155)
27	TOMMO_GENOMICS	ss5148145878	Apr 25, 2021 (155)
28	TOMMO_GENOMICS	ss5148145879	Apr 25, 2021 (155)
29	TOMMO_GENOMICS	ss5148145880	Apr 25, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5245574517	Oct 12, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5245574518	Oct 12, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5245574519	Oct 12, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5245574520	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5245574521	Oct 12, 2022 (156)
35	HUGCELL_USP	ss5446032363	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5446032364	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5446032365	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5446032366	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5446032367	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5446032368	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5675825574	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5675825575	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5675825577	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5675825578	Oct 12, 2022 (156)
45	EVA	ss5833171719	Oct 12, 2022 (156)
46	EVA	ss5833171720	Oct 12, 2022 (156)
47	EVA	ss5911714256	Oct 12, 2022 (156)
48	1000Genomes	NC_000001.10 - 207815356	Oct 11, 2018 (152)
49	The Danish reference pan genome	NC_000001.10 - 207815356	Apr 25, 2020 (154)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37743527 (NC_000001.11:207642010::T 32138/80186) Row 37743528 (NC_000001.11:207642010::TT 2156/80212) Row 37743529 (NC_000001.11:207642010::TTT 3172/80172)...	-	Apr 25, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 6115185 (NC_000001.10:207815355::T 10554/16012) Row 6115186 (NC_000001.10:207815355::TT 325/16012) Row 6115187 (NC_000001.10:207815355:T: 18/16012)	-	Apr 25, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 6115185 (NC_000001.10:207815355::T 10554/16012) Row 6115186 (NC_000001.10:207815355::TT 325/16012) Row 6115187 (NC_000001.10:207815355:T: 18/16012)	-	Apr 25, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 6115185 (NC_000001.10:207815355::T 10554/16012) Row 6115186 (NC_000001.10:207815355::TT 325/16012) Row 6115187 (NC_000001.10:207815355:T: 18/16012)	-	Apr 25, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 9662678 (NC_000001.11:207642010::T 19495/28024) Row 9662679 (NC_000001.11:207642010::TT 528/28024) Row 9662681 (NC_000001.11:207642010:T: 48/28024)...	-	Oct 12, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 9662678 (NC_000001.11:207642010::T 19495/28024) Row 9662679 (NC_000001.11:207642010::TT 528/28024) Row 9662681 (NC_000001.11:207642010:T: 48/28024)...	-	Oct 12, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 9662678 (NC_000001.11:207642010::T 19495/28024) Row 9662679 (NC_000001.11:207642010::TT 528/28024) Row 9662681 (NC_000001.11:207642010:T: 48/28024)...	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 9662678 (NC_000001.11:207642010::T 19495/28024) Row 9662679 (NC_000001.11:207642010::TT 528/28024) Row 9662681 (NC_000001.11:207642010:T: 48/28024)...	-	Oct 12, 2022 (156)
76	ALFA	NC_000001.11 - 207642011	Apr 25, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4010205026	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5237728, ss1367977084, ss3826610201	NC_000001.10:207815355:TTTTTTTTTTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3800261349, ss4010205025, ss5245574518, ss5446032368, ss5911714256	NC_000001.11:207642010:TTTTTTTTTTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4010205024	NC_000001.11:207642010:TTTTTTTTTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4010205023	NC_000001.11:207642010:TTTTTTTTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4010205022	NC_000001.11:207642010:TTTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss2988344893	NC_000001.10:207815355:TTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205021, ss5245574520, ss5446032366	NC_000001.11:207642010:TTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205020	NC_000001.11:207642010:TT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5148145880	NC_000001.10:207815355:T:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205019, ss5245574521, ss5446032367, ss5675825577	NC_000001.11:207642010:T:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95253280	NT_167186.1:1333157:T:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294622342	NC_000001.9:205881979::T	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
196121, ss1574085321, ss5148145878	NC_000001.10:207815355::T	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205007, ss5446032363, ss5675825574	NC_000001.11:207642010::T	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5148145879, ss5833171719	NC_000001.10:207815355::TT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205008, ss5245574519, ss5446032364, ss5675825575	NC_000001.11:207642010::TT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5833171720	NC_000001.10:207815355::TTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
ss4010205009, ss5245574517, ss5446032365, ss5675825578	NC_000001.11:207642010::TTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205010	NC_000001.11:207642010::TTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205011	NC_000001.11:207642010::TTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7587694216	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205012	NC_000001.11:207642010::TTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205013	NC_000001.11:207642010::TTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205014	NC_000001.11:207642010::TTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205015	NC_000001.11:207642010::TTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205016	NC_000001.11:207642010::TTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010205017	NC_000001.11:207642010::TTTTTTTTTT… NC_000001.11:207642010::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3101755711	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTT:	NC_000001.11:207642010:TTTTTTTTTTT… NC_000001.11:207642010:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

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

No publications for rs71154831

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

rs71154831