Name: rs1345601056
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.

rs1345601056

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:38410483-38410500 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.0000 (0/8360, ALFA)
delAA=0.0000 (0/8360, ALFA)
delA=0.0000 (0/8360, ALFA) (+ 3 more)
dupA=0.0000 (0/8360, ALFA)
dupAA=0.0000 (0/8360, ALFA)
delA=0.050 (28/556, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IGFBPL1 : 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	8360	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	4882	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	2358	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	86	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	2272	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	98	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	76	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	108	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	496	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	64	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	354	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	8360	(A)₁₈=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	4882	(A)₁₈=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	2358	(A)₁₈=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	496	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	354	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	108	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	98	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	64	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Northern Sweden	ACPOP	Study-wide	556	(A)₁₈=0.950	delA=0.050

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 9	NC_000009.12:g.38410498_38410500del
GRCh38.p14 chr 9	NC_000009.12:g.38410499_38410500del
GRCh38.p14 chr 9	NC_000009.12:g.38410500del
GRCh38.p14 chr 9	NC_000009.12:g.38410500dup
GRCh38.p14 chr 9	NC_000009.12:g.38410499_38410500dup
GRCh37.p13 chr 9	NC_000009.11:g.38410495_38410497del
GRCh37.p13 chr 9	NC_000009.11:g.38410496_38410497del
GRCh37.p13 chr 9	NC_000009.11:g.38410497del
GRCh37.p13 chr 9	NC_000009.11:g.38410497dup
GRCh37.p13 chr 9	NC_000009.11:g.38410496_38410497dup

Gene: IGFBPL1, insulin like growth factor binding protein like 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IGFBPL1 transcript	NM_001007563.3:c.9+906_… NM_001007563.3:c.9+906_9+908del	N/A	Intron Variant
IGFBPL1 transcript variant X1	XM_017014699.2:c.	N/A	Genic 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	(A)₁₈=	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 9	NC_000009.12:g.38410483_38410500=	NC_000009.12:g.38410498_38410500del	NC_000009.12:g.38410499_38410500del	NC_000009.12:g.38410500del	NC_000009.12:g.38410500dup	NC_000009.12:g.38410499_38410500dup
GRCh37.p13 chr 9	NC_000009.11:g.38410480_38410497=	NC_000009.11:g.38410495_38410497del	NC_000009.11:g.38410496_38410497del	NC_000009.11:g.38410497del	NC_000009.11:g.38410497dup	NC_000009.11:g.38410496_38410497dup
IGFBPL1 transcript	NM_001007563.2:c.*9+908=	NM_001007563.2:c.9+906_9+908del	NM_001007563.2:c.9+907_9+908del	NM_001007563.2:c.*9+908del	NM_001007563.2:c.*9+908dup	NM_001007563.2:c.9+907_9+908dup
IGFBPL1 transcript	NM_001007563.3:c.*9+908=	NM_001007563.3:c.9+906_9+908del	NM_001007563.3:c.9+907_9+908del	NM_001007563.3:c.*9+908del	NM_001007563.3:c.*9+908dup	NM_001007563.3:c.9+907_9+908dup

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#.

30 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3004741777	Nov 08, 2017 (151)
2	EVA_DECODE	ss3723907078	Jul 13, 2019 (153)
3	EVA_DECODE	ss3723907079	Jul 13, 2019 (153)
4	EVA_DECODE	ss3723907080	Jul 13, 2019 (153)
5	EVA_DECODE	ss3723907081	Jul 13, 2019 (153)
6	ACPOP	ss3736504414	Jul 13, 2019 (153)
7	EVA	ss3831653140	Apr 26, 2020 (154)
8	KOGIC	ss3965721430	Apr 26, 2020 (154)
9	KOGIC	ss3965721431	Apr 26, 2020 (154)
10	KOGIC	ss3965721432	Apr 26, 2020 (154)
11	KOGIC	ss3965721433	Apr 26, 2020 (154)
12	GNOMAD	ss4201392786	Apr 26, 2021 (155)
13	GNOMAD	ss4201392787	Apr 26, 2021 (155)
14	GNOMAD	ss4201392788	Apr 26, 2021 (155)
15	GNOMAD	ss4201392789	Apr 26, 2021 (155)
16	GNOMAD	ss4201392790	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5193078226	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5193078227	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5193078228	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5193078229	Apr 26, 2021 (155)
21	1000G_HIGH_COVERAGE	ss5280569841	Oct 13, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5280569842	Oct 13, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5280569843	Oct 13, 2022 (156)
24	HUGCELL_USP	ss5476767384	Oct 13, 2022 (156)
25	HUGCELL_USP	ss5476767386	Oct 13, 2022 (156)
26	HUGCELL_USP	ss5476767387	Oct 13, 2022 (156)
27	TOMMO_GENOMICS	ss5736412984	Oct 13, 2022 (156)
28	TOMMO_GENOMICS	ss5736412985	Oct 13, 2022 (156)
29	TOMMO_GENOMICS	ss5736412986	Oct 13, 2022 (156)
30	TOMMO_GENOMICS	ss5736412988	Oct 13, 2022 (156)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324586776 (NC_000009.12:38410482::A 6368/73104) Row 324586777 (NC_000009.12:38410482::AA 4/73200) Row 324586778 (NC_000009.12:38410482:A: 11630/73128)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324586776 (NC_000009.12:38410482::A 6368/73104) Row 324586777 (NC_000009.12:38410482::AA 4/73200) Row 324586778 (NC_000009.12:38410482:A: 11630/73128)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324586776 (NC_000009.12:38410482::A 6368/73104) Row 324586777 (NC_000009.12:38410482::AA 4/73200) Row 324586778 (NC_000009.12:38410482:A: 11630/73128)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324586776 (NC_000009.12:38410482::A 6368/73104) Row 324586777 (NC_000009.12:38410482::AA 4/73200) Row 324586778 (NC_000009.12:38410482:A: 11630/73128)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324586776 (NC_000009.12:38410482::A 6368/73104) Row 324586777 (NC_000009.12:38410482::AA 4/73200) Row 324586778 (NC_000009.12:38410482:A: 11630/73128)...	-	Apr 26, 2021 (155)
36	Korean Genome Project Submission ignored due to conflicting rows: Row 22099431 (NC_000009.12:38410484:A: 295/1816) Row 22099432 (NC_000009.12:38410485::A 94/1816) Row 22099433 (NC_000009.12:38410482:AAA: 3/1816)...	-	Apr 26, 2020 (154)
37	Korean Genome Project Submission ignored due to conflicting rows: Row 22099431 (NC_000009.12:38410484:A: 295/1816) Row 22099432 (NC_000009.12:38410485::A 94/1816) Row 22099433 (NC_000009.12:38410482:AAA: 3/1816)...	-	Apr 26, 2020 (154)
38	Korean Genome Project Submission ignored due to conflicting rows: Row 22099431 (NC_000009.12:38410484:A: 295/1816) Row 22099432 (NC_000009.12:38410485::A 94/1816) Row 22099433 (NC_000009.12:38410482:AAA: 3/1816)...	-	Apr 26, 2020 (154)
39	Korean Genome Project Submission ignored due to conflicting rows: Row 22099431 (NC_000009.12:38410484:A: 295/1816) Row 22099432 (NC_000009.12:38410485::A 94/1816) Row 22099433 (NC_000009.12:38410482:AAA: 3/1816)...	-	Apr 26, 2020 (154)
40	Northern Sweden	NC_000009.11 - 38410480	Jul 13, 2019 (153)
41	8.3KJPN Submission ignored due to conflicting rows: Row 51047533 (NC_000009.11:38410479::A 25/16666) Row 51047534 (NC_000009.11:38410479:A: 852/16666) Row 51047535 (NC_000009.11:38410479:AAA: 29/16666)...	-	Apr 26, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 51047533 (NC_000009.11:38410479::A 25/16666) Row 51047534 (NC_000009.11:38410479:A: 852/16666) Row 51047535 (NC_000009.11:38410479:AAA: 29/16666)...	-	Apr 26, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 51047533 (NC_000009.11:38410479::A 25/16666) Row 51047534 (NC_000009.11:38410479:A: 852/16666) Row 51047535 (NC_000009.11:38410479:AAA: 29/16666)...	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 51047533 (NC_000009.11:38410479::A 25/16666) Row 51047534 (NC_000009.11:38410479:A: 852/16666) Row 51047535 (NC_000009.11:38410479:AAA: 29/16666)...	-	Apr 26, 2021 (155)
45	14KJPN Submission ignored due to conflicting rows: Row 70250088 (NC_000009.12:38410482:A: 1485/28248) Row 70250089 (NC_000009.12:38410482::A 34/28248) Row 70250090 (NC_000009.12:38410482:AAA: 46/28248)...	-	Oct 13, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 70250088 (NC_000009.12:38410482:A: 1485/28248) Row 70250089 (NC_000009.12:38410482::A 34/28248) Row 70250090 (NC_000009.12:38410482:AAA: 46/28248)...	-	Oct 13, 2022 (156)
47	14KJPN Submission ignored due to conflicting rows: Row 70250088 (NC_000009.12:38410482:A: 1485/28248) Row 70250089 (NC_000009.12:38410482::A 34/28248) Row 70250090 (NC_000009.12:38410482:AAA: 46/28248)...	-	Oct 13, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 70250088 (NC_000009.12:38410482:A: 1485/28248) Row 70250089 (NC_000009.12:38410482::A 34/28248) Row 70250090 (NC_000009.12:38410482:AAA: 46/28248)...	-	Oct 13, 2022 (156)
49	ALFA	NC_000009.12 - 38410483	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
ss5193078228	NC_000009.11:38410479:AAA:	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3723907081, ss3965721432, ss4201392790, ss5280569843, ss5736412986	NC_000009.12:38410482:AAA:	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
6237686605	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4201392789, ss5476767387	NC_000009.12:38410482:AA:	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
6237686605	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3723907080, ss3965721433	NC_000009.12:38410483:AA:	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9789279, ss3004741777, ss3736504414, ss5193078227	NC_000009.11:38410479:A:	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4201392788, ss5280569841, ss5476767384, ss5736412984	NC_000009.12:38410482:A:	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
6237686605	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3723907079, ss3965721430	NC_000009.12:38410484:A:	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3831653140, ss5193078226	NC_000009.11:38410479::A	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4201392786, ss5280569842, ss5476767386, ss5736412985	NC_000009.12:38410482::A	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6237686605	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3723907078, ss3965721431	NC_000009.12:38410485::A	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5193078229	NC_000009.11:38410479::AA	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4201392787, ss5736412988	NC_000009.12:38410482::AA	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
6237686605	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000009.12:38410482:AAAAAAAAAAAA… NC_000009.12:38410482:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(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 rs1345601056

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

rs1345601056