Name: rs1491578632
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.

rs1491578632

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:19325766-19325776 (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: delTA / dupTA / dupTATA / dup(TA)₃…
delTA / dupTA / dupTATA / dup(TA)₃ / dup(TA)₄ / dup(TA)₅ / ins(TA)₆ / ins(TA)₇ / ins(TA)₈ / ins(TA)₉ / ins(TA)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: ins(TA)₉=0.000004 (1/264690, TOPMED)
dupTA=0.00000 (0/11860, ALFA)
dupTATA=0.00000 (0/11860, ALFA) (+ 8 more)
dup(TA)₃=0.00000 (0/11860, ALFA)
dup(TA)₄=0.00000 (0/11860, ALFA)
dup(TA)₅=0.00000 (0/11860, ALFA)
ins(TA)₆=0.00000 (0/11860, ALFA)
ins(TA)₇=0.00000 (0/11860, ALFA)
ins(TA)₈=0.00000 (0/11860, ALFA)
ins(TA)₉=0.00000 (0/11860, ALFA)
dupTATA=0.002 (1/548, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC24A3 : 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	11860	ATATATATATA=1.00000	ATATATATATATA=0.00000, ATATATATATATATA=0.00000, ATATATATATATATATA=0.00000, ATATATATATATATATATA=0.00000, ATATATATATATATATATATA=0.00000, ATATATATATATATATATATATA=0.00000, ATATATATATATATATATATATATA=0.00000, ATATATATATATATATATATATATATA=0.00000, ATATATATATATATATATATATATATATA=0.00000	1.0	N/A
European	Sub	7618	ATATATATATA=1.0000	ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATA=0.0000	1.0	N/A
African	Sub	2814	ATATATATATA=1.0000	ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATA=0.0000	1.0	N/A
African Others	Sub	108	ATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	1.0	N/A
African American	Sub	2706	ATATATATATA=1.0000	ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATA=0.0000	1.0	N/A
Asian	Sub	108	ATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	1.0	N/A
East Asian	Sub	84	ATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	1.0	N/A
Other Asian	Sub	24	ATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	1.0	N/A
Latin American 1	Sub	146	ATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	1.0	N/A
Latin American 2	Sub	610	ATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	1.0	N/A
South Asian	Sub	94	ATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00	1.0	N/A
Other	Sub	470	ATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	- No frequency provided	ins(TA)₉=0.000004
Allele Frequency Aggregator	Total	Global	11860	(AT)₅A=1.00000	dupTA=0.00000, dupTATA=0.00000, dup(TA)₃=0.00000, dup(TA)₄=0.00000, dup(TA)₅=0.00000, ins(TA)₆=0.00000, ins(TA)₇=0.00000, ins(TA)₈=0.00000, ins(TA)₉=0.00000
Allele Frequency Aggregator	European	Sub	7618	(AT)₅A=1.0000	dupTA=0.0000, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000, ins(TA)₆=0.0000, ins(TA)₇=0.0000, ins(TA)₈=0.0000, ins(TA)₉=0.0000
Allele Frequency Aggregator	African	Sub	2814	(AT)₅A=1.0000	dupTA=0.0000, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000, ins(TA)₆=0.0000, ins(TA)₇=0.0000, ins(TA)₈=0.0000, ins(TA)₉=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	(AT)₅A=1.000	dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, ins(TA)₆=0.000, ins(TA)₇=0.000, ins(TA)₈=0.000, ins(TA)₉=0.000
Allele Frequency Aggregator	Other	Sub	470	(AT)₅A=1.000	dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, ins(TA)₆=0.000, ins(TA)₇=0.000, ins(TA)₈=0.000, ins(TA)₉=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(AT)₅A=1.000	dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, ins(TA)₆=0.000, ins(TA)₇=0.000, ins(TA)₈=0.000, ins(TA)₉=0.000
Allele Frequency Aggregator	Asian	Sub	108	(AT)₅A=1.000	dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, ins(TA)₆=0.000, ins(TA)₇=0.000, ins(TA)₈=0.000, ins(TA)₉=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(AT)₅A=1.00	dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, ins(TA)₆=0.00, ins(TA)₇=0.00, ins(TA)₈=0.00, ins(TA)₉=0.00
Northern Sweden	ACPOP	Study-wide	548	- No frequency provided	dupTATA=0.002

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 20	NC_000020.11:g.19325767TA[4]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[6]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[7]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[8]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[9]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[10]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[11]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[12]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[13]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[14]
GRCh38.p14 chr 20	NC_000020.11:g.19325767TA[15]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[4]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[6]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[7]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[8]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[9]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[10]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[11]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[12]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[13]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[14]
GRCh37.p13 chr 20	NC_000020.10:g.19306411TA[15]

Gene: SLC24A3, solute carrier family 24 member 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC24A3 transcript	NM_020689.4:c.271+44679AT… NM_020689.4:c.271+44679AT[4]	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	(AT)₅A=	delTA	dupTA	dupTATA	dup(TA)₃	dup(TA)₄	dup(TA)₅	ins(TA)₆	ins(TA)₇	ins(TA)₈	ins(TA)₉	ins(TA)₁₀
GRCh38.p14 chr 20	NC_000020.11:g.19325766_19325776=	NC_000020.11:g.19325767TA[4]	NC_000020.11:g.19325767TA[6]	NC_000020.11:g.19325767TA[7]	NC_000020.11:g.19325767TA[8]	NC_000020.11:g.19325767TA[9]	NC_000020.11:g.19325767TA[10]	NC_000020.11:g.19325767TA[11]	NC_000020.11:g.19325767TA[12]	NC_000020.11:g.19325767TA[13]	NC_000020.11:g.19325767TA[14]	NC_000020.11:g.19325767TA[15]
GRCh37.p13 chr 20	NC_000020.10:g.19306410_19306420=	NC_000020.10:g.19306411TA[4]	NC_000020.10:g.19306411TA[6]	NC_000020.10:g.19306411TA[7]	NC_000020.10:g.19306411TA[8]	NC_000020.10:g.19306411TA[9]	NC_000020.10:g.19306411TA[10]	NC_000020.10:g.19306411TA[11]	NC_000020.10:g.19306411TA[12]	NC_000020.10:g.19306411TA[13]	NC_000020.10:g.19306411TA[14]	NC_000020.10:g.19306411TA[15]
SLC24A3 transcript	NM_020689.3:c.271+44679=	NM_020689.3:c.271+44679AT[4]	NM_020689.3:c.271+44679AT[6]	NM_020689.3:c.271+44679AT[7]	NM_020689.3:c.271+44679AT[8]	NM_020689.3:c.271+44679AT[9]	NM_020689.3:c.271+44679AT[10]	NM_020689.3:c.271+44679AT[11]	NM_020689.3:c.271+44679AT[12]	NM_020689.3:c.271+44679AT[13]	NM_020689.3:c.271+44679AT[14]	NM_020689.3:c.271+44679AT[15]
SLC24A3 transcript	NM_020689.4:c.271+44679=	NM_020689.4:c.271+44679AT[4]	NM_020689.4:c.271+44679AT[6]	NM_020689.4:c.271+44679AT[7]	NM_020689.4:c.271+44679AT[8]	NM_020689.4:c.271+44679AT[9]	NM_020689.4:c.271+44679AT[10]	NM_020689.4:c.271+44679AT[11]	NM_020689.4:c.271+44679AT[12]	NM_020689.4:c.271+44679AT[13]	NM_020689.4:c.271+44679AT[14]	NM_020689.4:c.271+44679AT[15]

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#.

27 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3706689465	Jul 13, 2019 (153)
2	EVA_DECODE	ss3706689466	Jul 13, 2019 (153)
3	EVA_DECODE	ss3706689467	Jul 13, 2019 (153)
4	EVA_DECODE	ss3706689468	Jul 13, 2019 (153)
5	ACPOP	ss3743308509	Jul 13, 2019 (153)
6	GNOMAD	ss4336161220	Apr 26, 2021 (155)
7	GNOMAD	ss4336161221	Apr 26, 2021 (155)
8	GNOMAD	ss4336161222	Apr 26, 2021 (155)
9	GNOMAD	ss4336161223	Apr 26, 2021 (155)
10	GNOMAD	ss4336161224	Apr 26, 2021 (155)
11	GNOMAD	ss4336161225	Apr 26, 2021 (155)
12	GNOMAD	ss4336161226	Apr 26, 2021 (155)
13	GNOMAD	ss4336161227	Apr 26, 2021 (155)
14	GNOMAD	ss4336161228	Apr 26, 2021 (155)
15	TOPMED	ss5084513945	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5229128260	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5229128261	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5229128262	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5229128263	Apr 26, 2021 (155)
20	1000G_HIGH_COVERAGE	ss5308309279	Oct 13, 2022 (156)
21	1000G_HIGH_COVERAGE	ss5308309280	Oct 13, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5308309281	Oct 13, 2022 (156)
23	HUGCELL_USP	ss5500690629	Oct 13, 2022 (156)
24	TOMMO_GENOMICS	ss5788195582	Oct 13, 2022 (156)
25	TOMMO_GENOMICS	ss5788195584	Oct 13, 2022 (156)
26	TOMMO_GENOMICS	ss5788195585	Oct 13, 2022 (156)
27	TOMMO_GENOMICS	ss5788195586	Oct 13, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548318241 (NC_000020.11:19325765::AT 122/39516) Row 548318242 (NC_000020.11:19325765::ATAT 59/39562) Row 548318243 (NC_000020.11:19325765::ATATAT 79/39418)...	-	Apr 26, 2021 (155)
37	Northern Sweden	NC_000020.10 - 19306410	Jul 13, 2019 (153)
38	8.3KJPN Submission ignored due to conflicting rows: Row 87097567 (NC_000020.10:19306409::ATATAT 19/16492) Row 87097568 (NC_000020.10:19306409::ATATATAT 9/16492) Row 87097569 (NC_000020.10:19306409::ATAT 44/16492)...	-	Apr 26, 2021 (155)
39	8.3KJPN Submission ignored due to conflicting rows: Row 87097567 (NC_000020.10:19306409::ATATAT 19/16492) Row 87097568 (NC_000020.10:19306409::ATATATAT 9/16492) Row 87097569 (NC_000020.10:19306409::ATAT 44/16492)...	-	Apr 26, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 87097567 (NC_000020.10:19306409::ATATAT 19/16492) Row 87097568 (NC_000020.10:19306409::ATATATAT 9/16492) Row 87097569 (NC_000020.10:19306409::ATAT 44/16492)...	-	Apr 26, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 87097567 (NC_000020.10:19306409::ATATAT 19/16492) Row 87097568 (NC_000020.10:19306409::ATATATAT 9/16492) Row 87097569 (NC_000020.10:19306409::ATAT 44/16492)...	-	Apr 26, 2021 (155)
42	14KJPN Submission ignored due to conflicting rows: Row 122032686 (NC_000020.11:19325765::AT 126/27980) Row 122032688 (NC_000020.11:19325765::ATATATAT 17/27980) Row 122032689 (NC_000020.11:19325765::ATATAT 21/27980)...	-	Oct 13, 2022 (156)
43	14KJPN Submission ignored due to conflicting rows: Row 122032686 (NC_000020.11:19325765::AT 126/27980) Row 122032688 (NC_000020.11:19325765::ATATATAT 17/27980) Row 122032689 (NC_000020.11:19325765::ATATAT 21/27980)...	-	Oct 13, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 122032686 (NC_000020.11:19325765::AT 126/27980) Row 122032688 (NC_000020.11:19325765::ATATATAT 17/27980) Row 122032689 (NC_000020.11:19325765::ATATAT 21/27980)...	-	Oct 13, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 122032686 (NC_000020.11:19325765::AT 126/27980) Row 122032688 (NC_000020.11:19325765::ATATATAT 17/27980) Row 122032689 (NC_000020.11:19325765::ATATAT 21/27980)...	-	Oct 13, 2022 (156)
46	TopMed	NC_000020.11 - 19325766	Apr 26, 2021 (155)
47	ALFA	NC_000020.11 - 19325766	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3706689465	NC_000020.11:19325774:TA:	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATA	(self)
ss5229128263	NC_000020.10:19306409::AT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATA	(self)
ss4336161220, ss5308309279, ss5788195582	NC_000020.11:19325765::AT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATA	(self)
ss3706689466	NC_000020.11:19325776::TA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATA	(self)
16593374, ss3743308509, ss5229128262	NC_000020.10:19306409::ATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATA	(self)
ss4336161221, ss5788195586	NC_000020.11:19325765::ATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATA	(self)
ss3706689467	NC_000020.11:19325776::TATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATA	(self)
ss5229128260	NC_000020.10:19306409::ATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATA	(self)
ss4336161222, ss5308309280, ss5500690629, ss5788195585	NC_000020.11:19325765::ATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATA	(self)
ss5229128261	NC_000020.10:19306409::ATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATA	(self)
ss4336161223, ss5308309281, ss5788195584	NC_000020.11:19325765::ATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATA	(self)
ss3706689468	NC_000020.11:19325776::TATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATA	(self)
ss4336161224	NC_000020.11:19325765::ATATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATA	(self)
ss4336161225	NC_000020.11:19325765::ATATATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATA	(self)
ss4336161226	NC_000020.11:19325765::ATATATATATA… NC_000020.11:19325765::ATATATATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATA	(self)
ss4336161227	NC_000020.11:19325765::ATATATATATA… NC_000020.11:19325765::ATATATATATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATATA	(self)
359622890, ss5084513945	NC_000020.11:19325765::ATATATATATA… NC_000020.11:19325765::ATATATATATATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATATATA	(self)
1869436338	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATATATA	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATATATA	(self)
ss4336161228	NC_000020.11:19325765::ATATATATATA… NC_000020.11:19325765::ATATATATATATATATATAT	NC_000020.11:19325765:ATATATATATA:… NC_000020.11:19325765:ATATATATATA:ATATATATATATATATATATATATATATATA	(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 rs1491578632

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491578632