Name: rs10528850
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.

rs10528850

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:68238587-68238603 (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: delCACA / delCA / dupCA / dupCACA …
delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄ / dup(CA)₅ / dup(CA)₆ / dup(CA)₇ / dup(CA)₈
Variation Type: Indel Insertion and Deletion
Frequency: dup(CA)₄=0.1900 (1359/7154, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: AMZ2 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	7154	ACACACACACACACACA=0.6992	ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACACA=0.1039, ACACACACACACACACACACA=0.0001, ACACACACACACACACACACACA=0.0067, ACACACACACACACACACACACACA=0.1900, ACACACACACACACACACACACACACA=0.0001, ACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000	0.679564	0.067534	0.252902	32
European	Sub	6706	ACACACACACACACACA=0.6797	ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACACA=0.1105, ACACACACACACACACACACA=0.0001, ACACACACACACACACACACACA=0.0072, ACACACACACACACACACACACACA=0.2024, ACACACACACACACACACACACACACA=0.0001, ACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000	0.652804	0.073254	0.273941	32
African	Sub	188	ACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	2	ACACACACACACACACA=1.0	ACACACACACACA=0.0, ACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
African American	Sub	186	ACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	12	ACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	12	ACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	0	ACACACACACACACACA=0	ACACACACACACA=0, ACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0, ACACACACACACACACACACACA=0, ACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACA=0	0	0	0	N/A
Latin American 1	Sub	40	ACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	90	ACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	30	ACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other	Sub	88	ACACACACACACACACA=0.95	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACACA=0.02, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.02, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00	0.97619	0.0	0.02381	0

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	7154	(AC)₈A=0.6992	delCACA=0.0000, delCA=0.0000, dupCA=0.1039, dupCACA=0.0001, dup(CA)₃=0.0067, dup(CA)₄=0.1900, dup(CA)₅=0.0001, dup(CA)₆=0.0000, dup(CA)₇=0.0000, dup(CA)₈=0.0000
Allele Frequency Aggregator	European	Sub	6706	(AC)₈A=0.6797	delCACA=0.0000, delCA=0.0000, dupCA=0.1105, dupCACA=0.0001, dup(CA)₃=0.0072, dup(CA)₄=0.2024, dup(CA)₅=0.0001, dup(CA)₆=0.0000, dup(CA)₇=0.0000, dup(CA)₈=0.0000
Allele Frequency Aggregator	African	Sub	188	(AC)₈A=1.000	delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000, dup(CA)₇=0.000, dup(CA)₈=0.000
Allele Frequency Aggregator	Latin American 2	Sub	90	(AC)₈A=1.00	delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00
Allele Frequency Aggregator	Other	Sub	88	(AC)₈A=0.95	delCACA=0.00, delCA=0.00, dupCA=0.02, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.02, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	40	(AC)₈A=1.00	delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(AC)₈A=1.00	delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00
Allele Frequency Aggregator	Asian	Sub	12	(AC)₈A=1.00	delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00

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 17	NC_000017.11:g.68238588CA[6]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[7]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[9]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[10]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[11]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[12]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[13]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[14]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[15]
GRCh38.p14 chr 17	NC_000017.11:g.68238588CA[16]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[6]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[7]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[9]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[10]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[11]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[12]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[13]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[14]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[15]
GRCh37.p13 chr 17	NC_000017.10:g.66234729CA[16]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[6]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[7]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[9]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[10]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[11]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[12]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[13]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[14]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[15]
AMZ2 RefSeqGene	NG_051827.1:g.37460CA[16]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[6]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[7]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[9]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[10]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[11]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[12]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[13]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[14]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[15]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298599CA[16]

Gene: AMZ2, archaelysin family metallopeptidase 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
AMZ2 transcript variant 9	NM_001346471.1:c.1-11601A… NM_001346471.1:c.1-11601AC[6]	N/A	Intron Variant
AMZ2 transcript variant 10	NM_001346472.1:c.-1+10967… NM_001346472.1:c.-1+10967AC[6]	N/A	Intron Variant
AMZ2 transcript variant 11	NM_001346473.1:c.-66-1005… NM_001346473.1:c.-66-10053AC[6]	N/A	Intron Variant
AMZ2 transcript variant 18	NM_001346480.1:c.1-11601A… NM_001346480.1:c.1-11601AC[6]	N/A	Intron Variant
AMZ2 transcript variant 19	NM_001346481.1:c.-112-116… NM_001346481.1:c.-112-11601AC[6]	N/A	Intron Variant
AMZ2 transcript variant 2	NM_001033569.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 3	NM_001033570.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 4	NM_001033571.1:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 5	NM_001033572.1:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 6	NM_001033574.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 7	NM_001289054.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 8	NM_001289056.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 12	NM_001346474.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 13	NM_001346475.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 14	NM_001346476.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 15	NM_001346477.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 16	NM_001346478.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 17	NM_001346479.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 20	NM_001346482.1:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 21	NM_001346483.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 22	NM_001346484.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 23	NM_001346485.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 1	NM_016627.5:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 24	NR_144442.2:n.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant 25	NR_144443.2:n.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant X4	XM_024450788.2:c.-62-1005… XM_024450788.2:c.-62-10057AC[6]	N/A	Intron Variant
AMZ2 transcript variant X1	XM_047436210.1:c.-66-1005… XM_047436210.1:c.-66-10053AC[6]	N/A	Intron Variant
AMZ2 transcript variant X2	XM_024450786.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant X3	XM_024450787.2:c.	N/A	Genic Upstream Transcript Variant
AMZ2 transcript variant X5	XM_047436211.1:c.	N/A	Genic Upstream 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	(AC)₈A=	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄	dup(CA)₅	dup(CA)₆	dup(CA)₇	dup(CA)₈
GRCh38.p14 chr 17	NC_000017.11:g.68238587_68238603=	NC_000017.11:g.68238588CA[6]	NC_000017.11:g.68238588CA[7]	NC_000017.11:g.68238588CA[9]	NC_000017.11:g.68238588CA[10]	NC_000017.11:g.68238588CA[11]	NC_000017.11:g.68238588CA[12]	NC_000017.11:g.68238588CA[13]	NC_000017.11:g.68238588CA[14]	NC_000017.11:g.68238588CA[15]	NC_000017.11:g.68238588CA[16]
GRCh37.p13 chr 17	NC_000017.10:g.66234728_66234744=	NC_000017.10:g.66234729CA[6]	NC_000017.10:g.66234729CA[7]	NC_000017.10:g.66234729CA[9]	NC_000017.10:g.66234729CA[10]	NC_000017.10:g.66234729CA[11]	NC_000017.10:g.66234729CA[12]	NC_000017.10:g.66234729CA[13]	NC_000017.10:g.66234729CA[14]	NC_000017.10:g.66234729CA[15]	NC_000017.10:g.66234729CA[16]
AMZ2 RefSeqGene	NG_051827.1:g.37459_37475=	NG_051827.1:g.37460CA[6]	NG_051827.1:g.37460CA[7]	NG_051827.1:g.37460CA[9]	NG_051827.1:g.37460CA[10]	NG_051827.1:g.37460CA[11]	NG_051827.1:g.37460CA[12]	NG_051827.1:g.37460CA[13]	NG_051827.1:g.37460CA[14]	NG_051827.1:g.37460CA[15]	NG_051827.1:g.37460CA[16]
GRCh37.p13 chr 17 fix patch HG747_PATCH	NW_003871088.1:g.298598_298614=	NW_003871088.1:g.298599CA[6]	NW_003871088.1:g.298599CA[7]	NW_003871088.1:g.298599CA[9]	NW_003871088.1:g.298599CA[10]	NW_003871088.1:g.298599CA[11]	NW_003871088.1:g.298599CA[12]	NW_003871088.1:g.298599CA[13]	NW_003871088.1:g.298599CA[14]	NW_003871088.1:g.298599CA[15]	NW_003871088.1:g.298599CA[16]
AMZ2 transcript variant 9	NM_001346471.1:c.1-11601=	NM_001346471.1:c.1-11601AC[6]	NM_001346471.1:c.1-11601AC[7]	NM_001346471.1:c.1-11601AC[9]	NM_001346471.1:c.1-11601AC[10]	NM_001346471.1:c.1-11601AC[11]	NM_001346471.1:c.1-11601AC[12]	NM_001346471.1:c.1-11601AC[13]	NM_001346471.1:c.1-11601AC[14]	NM_001346471.1:c.1-11601AC[15]	NM_001346471.1:c.1-11601AC[16]
AMZ2 transcript variant 10	NM_001346472.1:c.-1+10967=	NM_001346472.1:c.-1+10967AC[6]	NM_001346472.1:c.-1+10967AC[7]	NM_001346472.1:c.-1+10967AC[9]	NM_001346472.1:c.-1+10967AC[10]	NM_001346472.1:c.-1+10967AC[11]	NM_001346472.1:c.-1+10967AC[12]	NM_001346472.1:c.-1+10967AC[13]	NM_001346472.1:c.-1+10967AC[14]	NM_001346472.1:c.-1+10967AC[15]	NM_001346472.1:c.-1+10967AC[16]
AMZ2 transcript variant 11	NM_001346473.1:c.-66-10053=	NM_001346473.1:c.-66-10053AC[6]	NM_001346473.1:c.-66-10053AC[7]	NM_001346473.1:c.-66-10053AC[9]	NM_001346473.1:c.-66-10053AC[10]	NM_001346473.1:c.-66-10053AC[11]	NM_001346473.1:c.-66-10053AC[12]	NM_001346473.1:c.-66-10053AC[13]	NM_001346473.1:c.-66-10053AC[14]	NM_001346473.1:c.-66-10053AC[15]	NM_001346473.1:c.-66-10053AC[16]
AMZ2 transcript variant 18	NM_001346480.1:c.1-11601=	NM_001346480.1:c.1-11601AC[6]	NM_001346480.1:c.1-11601AC[7]	NM_001346480.1:c.1-11601AC[9]	NM_001346480.1:c.1-11601AC[10]	NM_001346480.1:c.1-11601AC[11]	NM_001346480.1:c.1-11601AC[12]	NM_001346480.1:c.1-11601AC[13]	NM_001346480.1:c.1-11601AC[14]	NM_001346480.1:c.1-11601AC[15]	NM_001346480.1:c.1-11601AC[16]
AMZ2 transcript variant 19	NM_001346481.1:c.-112-11601=	NM_001346481.1:c.-112-11601AC[6]	NM_001346481.1:c.-112-11601AC[7]	NM_001346481.1:c.-112-11601AC[9]	NM_001346481.1:c.-112-11601AC[10]	NM_001346481.1:c.-112-11601AC[11]	NM_001346481.1:c.-112-11601AC[12]	NM_001346481.1:c.-112-11601AC[13]	NM_001346481.1:c.-112-11601AC[14]	NM_001346481.1:c.-112-11601AC[15]	NM_001346481.1:c.-112-11601AC[16]
AMZ2 transcript variant X1	XM_005257432.1:c.193-11601=	XM_005257432.1:c.193-11601AC[6]	XM_005257432.1:c.193-11601AC[7]	XM_005257432.1:c.193-11601AC[9]	XM_005257432.1:c.193-11601AC[10]	XM_005257432.1:c.193-11601AC[11]	XM_005257432.1:c.193-11601AC[12]	XM_005257432.1:c.193-11601AC[13]	XM_005257432.1:c.193-11601AC[14]	XM_005257432.1:c.193-11601AC[15]	XM_005257432.1:c.193-11601AC[16]
AMZ2 transcript variant X7	XM_005257438.1:c.193-11601=	XM_005257438.1:c.193-11601AC[6]	XM_005257438.1:c.193-11601AC[7]	XM_005257438.1:c.193-11601AC[9]	XM_005257438.1:c.193-11601AC[10]	XM_005257438.1:c.193-11601AC[11]	XM_005257438.1:c.193-11601AC[12]	XM_005257438.1:c.193-11601AC[13]	XM_005257438.1:c.193-11601AC[14]	XM_005257438.1:c.193-11601AC[15]	XM_005257438.1:c.193-11601AC[16]
AMZ2 transcript variant X1	XM_005277777.1:c.193-11601=	XM_005277777.1:c.193-11601AC[6]	XM_005277777.1:c.193-11601AC[7]	XM_005277777.1:c.193-11601AC[9]	XM_005277777.1:c.193-11601AC[10]	XM_005277777.1:c.193-11601AC[11]	XM_005277777.1:c.193-11601AC[12]	XM_005277777.1:c.193-11601AC[13]	XM_005277777.1:c.193-11601AC[14]	XM_005277777.1:c.193-11601AC[15]	XM_005277777.1:c.193-11601AC[16]
AMZ2 transcript variant X7	XM_005277783.1:c.193-11601=	XM_005277783.1:c.193-11601AC[6]	XM_005277783.1:c.193-11601AC[7]	XM_005277783.1:c.193-11601AC[9]	XM_005277783.1:c.193-11601AC[10]	XM_005277783.1:c.193-11601AC[11]	XM_005277783.1:c.193-11601AC[12]	XM_005277783.1:c.193-11601AC[13]	XM_005277783.1:c.193-11601AC[14]	XM_005277783.1:c.193-11601AC[15]	XM_005277783.1:c.193-11601AC[16]
AMZ2 transcript variant X4	XM_024450788.2:c.-62-10057=	XM_024450788.2:c.-62-10057AC[6]	XM_024450788.2:c.-62-10057AC[7]	XM_024450788.2:c.-62-10057AC[9]	XM_024450788.2:c.-62-10057AC[10]	XM_024450788.2:c.-62-10057AC[11]	XM_024450788.2:c.-62-10057AC[12]	XM_024450788.2:c.-62-10057AC[13]	XM_024450788.2:c.-62-10057AC[14]	XM_024450788.2:c.-62-10057AC[15]	XM_024450788.2:c.-62-10057AC[16]
AMZ2 transcript variant X1	XM_047436210.1:c.-66-10053=	XM_047436210.1:c.-66-10053AC[6]	XM_047436210.1:c.-66-10053AC[7]	XM_047436210.1:c.-66-10053AC[9]	XM_047436210.1:c.-66-10053AC[10]	XM_047436210.1:c.-66-10053AC[11]	XM_047436210.1:c.-66-10053AC[12]	XM_047436210.1:c.-66-10053AC[13]	XM_047436210.1:c.-66-10053AC[14]	XM_047436210.1:c.-66-10053AC[15]	XM_047436210.1:c.-66-10053AC[16]

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#.

72 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83703726	Dec 15, 2007 (130)
2	HGSV	ss83752460	Dec 15, 2007 (130)
3	HUMANGENOME_JCVI	ss95699395	Feb 06, 2009 (130)
4	BUSHMAN	ss193458464	Jul 04, 2010 (132)
5	GMI	ss289335506	May 04, 2012 (137)
6	1000GENOMES	ss327802135	May 09, 2011 (136)
7	1000GENOMES	ss327929327	May 09, 2011 (136)
8	1000GENOMES	ss328227997	May 09, 2011 (136)
9	LUNTER	ss552538418	Apr 25, 2013 (138)
10	LUNTER	ss552894738	Apr 25, 2013 (138)
11	LUNTER	ss553624668	Apr 25, 2013 (138)
12	SSMP	ss664371990	Apr 09, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1708828138	Apr 09, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1708828139	Apr 09, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1708828246	Apr 09, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1708828247	Apr 09, 2015 (144)
17	HAMMER_LAB	ss1808857319	Sep 11, 2015 (146)
18	SWEGEN	ss3015819330	Oct 12, 2018 (152)
19	MCHAISSO	ss3064718686	Nov 08, 2017 (151)
20	URBANLAB	ss3650690501	Oct 12, 2018 (152)
21	ACPOP	ss3742170989	Jul 13, 2019 (153)
22	ACPOP	ss3742170990	Jul 13, 2019 (153)
23	ACPOP	ss3742170991	Jul 13, 2019 (153)
24	PACBIO	ss3788253042	Jul 13, 2019 (153)
25	PACBIO	ss3788253043	Jul 13, 2019 (153)
26	PACBIO	ss3793200644	Jul 13, 2019 (153)
27	PACBIO	ss3793200645	Jul 13, 2019 (153)
28	PACBIO	ss3798086597	Jul 13, 2019 (153)
29	PACBIO	ss3798086598	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3820135394	Jul 13, 2019 (153)
31	EVA	ss3834951366	Apr 27, 2020 (154)
32	EVA	ss3841087711	Apr 27, 2020 (154)
33	EVA	ss3846585661	Apr 27, 2020 (154)
34	KOGIC	ss3979191863	Apr 27, 2020 (154)
35	KOGIC	ss3979191864	Apr 27, 2020 (154)
36	KOGIC	ss3979191865	Apr 27, 2020 (154)
37	KOGIC	ss3979191866	Apr 27, 2020 (154)
38	KOGIC	ss3979191867	Apr 27, 2020 (154)
39	GNOMAD	ss4314780042	Apr 27, 2021 (155)
40	GNOMAD	ss4314780043	Apr 27, 2021 (155)
41	GNOMAD	ss4314780044	Apr 27, 2021 (155)
42	GNOMAD	ss4314780045	Apr 27, 2021 (155)
43	GNOMAD	ss4314780046	Apr 27, 2021 (155)
44	GNOMAD	ss4314780047	Apr 27, 2021 (155)
45	GNOMAD	ss4314780048	Apr 27, 2021 (155)
46	GNOMAD	ss4314780052	Apr 27, 2021 (155)
47	GNOMAD	ss4314780053	Apr 27, 2021 (155)
48	TOMMO_GENOMICS	ss5223239582	Apr 27, 2021 (155)
49	TOMMO_GENOMICS	ss5223239583	Apr 27, 2021 (155)
50	TOMMO_GENOMICS	ss5223239584	Apr 27, 2021 (155)
51	TOMMO_GENOMICS	ss5223239585	Apr 27, 2021 (155)
52	TOMMO_GENOMICS	ss5223239586	Apr 27, 2021 (155)
53	1000G_HIGH_COVERAGE	ss5303750945	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5303750946	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5303750947	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5303750948	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5303750949	Oct 16, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5303750950	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5496732184	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5496732185	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5496732186	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5496732187	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5496732188	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5496732189	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5779713204	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5779713205	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5779713206	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5779713207	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5779713208	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5779713209	Oct 16, 2022 (156)
71	EVA	ss5834216193	Oct 16, 2022 (156)
72	EVA	ss5834216194	Oct 16, 2022 (156)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40231961 (NC_000017.10:66234727::ACACACAC 1239/3854) Row 40231962 (NC_000017.10:66234727::AC 504/3854)	-	Oct 12, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40231961 (NC_000017.10:66234727::ACACACAC 1239/3854) Row 40231962 (NC_000017.10:66234727::AC 504/3854)	-	Oct 12, 2018 (152)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512407269 (NC_000017.11:68238586::AC 16468/138924) Row 512407270 (NC_000017.11:68238586::ACAC 33/139000) Row 512407271 (NC_000017.11:68238586::ACACAC 9798/138820)...	-	Apr 27, 2021 (155)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 35569864 (NC_000017.11:68238586::AC 528/1832) Row 35569865 (NC_000017.11:68238586::ACACACAC 412/1832) Row 35569866 (NC_000017.11:68238586::ACACAC 204/1832)...	-	Apr 27, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 35569864 (NC_000017.11:68238586::AC 528/1832) Row 35569865 (NC_000017.11:68238586::ACACACAC 412/1832) Row 35569866 (NC_000017.11:68238586::ACACAC 204/1832)...	-	Apr 27, 2020 (154)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 35569864 (NC_000017.11:68238586::AC 528/1832) Row 35569865 (NC_000017.11:68238586::ACACACAC 412/1832) Row 35569866 (NC_000017.11:68238586::ACACAC 204/1832)...	-	Apr 27, 2020 (154)
87	Korean Genome Project Submission ignored due to conflicting rows: Row 35569864 (NC_000017.11:68238586::AC 528/1832) Row 35569865 (NC_000017.11:68238586::ACACACAC 412/1832) Row 35569866 (NC_000017.11:68238586::ACACAC 204/1832)...	-	Apr 27, 2020 (154)
88	Korean Genome Project Submission ignored due to conflicting rows: Row 35569864 (NC_000017.11:68238586::AC 528/1832) Row 35569865 (NC_000017.11:68238586::ACACACAC 412/1832) Row 35569866 (NC_000017.11:68238586::ACACAC 204/1832)...	-	Apr 27, 2020 (154)
89	Northern Sweden Submission ignored due to conflicting rows: Row 15455854 (NC_000017.10:66234727::ACACACAC 189/600) Row 15455855 (NC_000017.10:66234727::AC 60/600) Row 15455856 (NC_000017.10:66234727::ACACAC 6/600)	-	Jul 13, 2019 (153)
90	Northern Sweden Submission ignored due to conflicting rows: Row 15455854 (NC_000017.10:66234727::ACACACAC 189/600) Row 15455855 (NC_000017.10:66234727::AC 60/600) Row 15455856 (NC_000017.10:66234727::ACACAC 6/600)	-	Jul 13, 2019 (153)
91	Northern Sweden Submission ignored due to conflicting rows: Row 15455854 (NC_000017.10:66234727::ACACACAC 189/600) Row 15455855 (NC_000017.10:66234727::AC 60/600) Row 15455856 (NC_000017.10:66234727::ACACAC 6/600)	-	Jul 13, 2019 (153)
92	8.3KJPN Submission ignored due to conflicting rows: Row 81208889 (NC_000017.10:66234727::AC 4056/16760) Row 81208890 (NC_000017.10:66234727::ACACAC 1643/16760) Row 81208891 (NC_000017.10:66234727::ACAC 645/16760)...	-	Apr 27, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 81208889 (NC_000017.10:66234727::AC 4056/16760) Row 81208890 (NC_000017.10:66234727::ACACAC 1643/16760) Row 81208891 (NC_000017.10:66234727::ACAC 645/16760)...	-	Apr 27, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 81208889 (NC_000017.10:66234727::AC 4056/16760) Row 81208890 (NC_000017.10:66234727::ACACAC 1643/16760) Row 81208891 (NC_000017.10:66234727::ACAC 645/16760)...	-	Apr 27, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 81208889 (NC_000017.10:66234727::AC 4056/16760) Row 81208890 (NC_000017.10:66234727::ACACAC 1643/16760) Row 81208891 (NC_000017.10:66234727::ACAC 645/16760)...	-	Apr 27, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 81208889 (NC_000017.10:66234727::AC 4056/16760) Row 81208890 (NC_000017.10:66234727::ACACAC 1643/16760) Row 81208891 (NC_000017.10:66234727::ACAC 645/16760)...	-	Apr 27, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 113550308 (NC_000017.11:68238586::AC 6921/28258) Row 113550309 (NC_000017.11:68238586::ACACACAC 5826/28258) Row 113550310 (NC_000017.11:68238586::ACACAC 2808/28258)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 113550308 (NC_000017.11:68238586::AC 6921/28258) Row 113550309 (NC_000017.11:68238586::ACACACAC 5826/28258) Row 113550310 (NC_000017.11:68238586::ACACAC 2808/28258)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 113550308 (NC_000017.11:68238586::AC 6921/28258) Row 113550309 (NC_000017.11:68238586::ACACACAC 5826/28258) Row 113550310 (NC_000017.11:68238586::ACACAC 2808/28258)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 113550308 (NC_000017.11:68238586::AC 6921/28258) Row 113550309 (NC_000017.11:68238586::ACACACAC 5826/28258) Row 113550310 (NC_000017.11:68238586::ACACAC 2808/28258)...	-	Oct 16, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 113550308 (NC_000017.11:68238586::AC 6921/28258) Row 113550309 (NC_000017.11:68238586::ACACACAC 5826/28258) Row 113550310 (NC_000017.11:68238586::ACACAC 2808/28258)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 113550308 (NC_000017.11:68238586::AC 6921/28258) Row 113550309 (NC_000017.11:68238586::ACACACAC 5826/28258) Row 113550310 (NC_000017.11:68238586::ACACAC 2808/28258)...	-	Oct 16, 2022 (156)
103	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40231961 (NC_000017.10:66234727::ACACACAC 1141/3708) Row 40231962 (NC_000017.10:66234727::AC 505/3708)	-	Oct 12, 2018 (152)
104	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40231961 (NC_000017.10:66234727::ACACACAC 1141/3708) Row 40231962 (NC_000017.10:66234727::AC 505/3708)	-	Oct 12, 2018 (152)
105	ALFA	NC_000017.11 - 68238587	Apr 27, 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)
rs147894949	Oct 19, 2011 (136)
rs149774780	Oct 19, 2011 (136)
rs60893729	May 26, 2008 (130)
rs376981488	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3015819330	NC_000017.10:66234727:ACAC:	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACA	(self)
ss4314780053	NC_000017.11:68238586:ACAC:	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACA	(self)
ss4314780052, ss5779713208	NC_000017.11:68238586:AC:	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACA	(self)
ss327802135, ss553624668	NC_000017.9:63746322::AC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACA	(self)
ss289335506	NC_000017.9:63746339::CA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACA	(self)
ss664371990, ss1708828139, ss1708828247, ss3742170990, ss3788253042, ss3793200644, ss3798086597, ss5223239582, ss5834216194	NC_000017.10:66234727::AC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACA	(self)
ss3820135394, ss3979191863, ss4314780042, ss5303750945, ss5496732189, ss5779713204	NC_000017.11:68238586::AC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACA	(self)
ss5223239584	NC_000017.10:66234727::ACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3979191866, ss4314780043, ss5496732187, ss5779713207	NC_000017.11:68238586::ACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACA	(self)
ss552894738	NC_000017.9:63746322::ACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss1808857319, ss3742170991, ss5223239583	NC_000017.10:66234727::ACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3979191865, ss4314780044, ss5303750947, ss5496732188, ss5779713206	NC_000017.11:68238586::ACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss193458464	NT_010783.16:41302606::ACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss327929327, ss328227997, ss552538418	NC_000017.9:63746322::ACACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss1708828138, ss1708828246, ss3742170989, ss3788253043, ss3793200645, ss3798086598, ss3834951366, ss3841087711, ss5223239585, ss5834216193	NC_000017.10:66234727::ACACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3064718686, ss3650690501, ss3846585661, ss3979191864, ss4314780045, ss5303750946, ss5496732184, ss5779713205	NC_000017.11:68238586::ACACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss83703726, ss83752460, ss95699395	NT_010783.15:31508896::CACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss5223239586	NC_000017.10:66234727::ACACACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3979191867, ss4314780046, ss5303750948, ss5496732185, ss5779713209	NC_000017.11:68238586::ACACACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss4314780047, ss5303750949, ss5496732186	NC_000017.11:68238586::ACACACACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss4314780048, ss5303750950	NC_000017.11:68238586::ACACACACACA… NC_000017.11:68238586::ACACACACACACAC	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
11184573580	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACACACA	NC_000017.11:68238586:ACACACACACAC… NC_000017.11:68238586:ACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)

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

No publications for rs10528850

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

rs10528850