Name: rs72123421
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.

rs72123421

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:93882448-93882463 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₆ / del(A)₄ / delAAA / delAA…
del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₁₀ / ins(A)₁₇
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₆=0.0000 (0/2866, ALFA)
del(A)₄=0.0000 (0/2866, ALFA)
delAAA=0.0000 (0/2866, ALFA) (+ 5 more)
delAA=0.0000 (0/2866, ALFA)
delA=0.0000 (0/2866, ALFA)
dupA=0.0000 (0/2866, ALFA)
dupAA=0.0000 (0/2866, ALFA)
dupAAA=0.0000 (0/2866, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	2866	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1984	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	388	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	6	AAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	382	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	58	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	46	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	38	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	236	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	40	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	122	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=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
Allele Frequency Aggregator	Total	Global	2866	(A)₁₆=1.0000	del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	1984	(A)₁₆=1.0000	del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	388	(A)₁₆=1.000	del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	236	(A)₁₆=1.000	del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	122	(A)₁₆=1.000	del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Asian	Sub	58	(A)₁₆=1.00	del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	40	(A)₁₆=1.00	del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	38	(A)₁₆=1.00	del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00

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 15	NC_000015.10:g.93882458_93882463del
GRCh38.p14 chr 15	NC_000015.10:g.93882460_93882463del
GRCh38.p14 chr 15	NC_000015.10:g.93882461_93882463del
GRCh38.p14 chr 15	NC_000015.10:g.93882462_93882463del
GRCh38.p14 chr 15	NC_000015.10:g.93882463del
GRCh38.p14 chr 15	NC_000015.10:g.93882463dup
GRCh38.p14 chr 15	NC_000015.10:g.93882462_93882463dup
GRCh38.p14 chr 15	NC_000015.10:g.93882461_93882463dup
GRCh38.p14 chr 15	NC_000015.10:g.93882454_93882463dup
GRCh38.p14 chr 15	NC_000015.10:g.93882463_93882464insAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.94425687_94425692del
GRCh37.p13 chr 15	NC_000015.9:g.94425689_94425692del
GRCh37.p13 chr 15	NC_000015.9:g.94425690_94425692del
GRCh37.p13 chr 15	NC_000015.9:g.94425691_94425692del
GRCh37.p13 chr 15	NC_000015.9:g.94425692del
GRCh37.p13 chr 15	NC_000015.9:g.94425692dup
GRCh37.p13 chr 15	NC_000015.9:g.94425691_94425692dup
GRCh37.p13 chr 15	NC_000015.9:g.94425690_94425692dup
GRCh37.p13 chr 15	NC_000015.9:g.94425683_94425692dup
GRCh37.p13 chr 15	NC_000015.9:g.94425692_94425693insAAAAAAAAAAAAAAAAA

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)₁₆=	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₁₀	ins(A)₁₇
GRCh38.p14 chr 15	NC_000015.10:g.93882448_93882463=	NC_000015.10:g.93882458_93882463del	NC_000015.10:g.93882460_93882463del	NC_000015.10:g.93882461_93882463del	NC_000015.10:g.93882462_93882463del	NC_000015.10:g.93882463del	NC_000015.10:g.93882463dup	NC_000015.10:g.93882462_93882463dup	NC_000015.10:g.93882461_93882463dup	NC_000015.10:g.93882454_93882463dup	NC_000015.10:g.93882463_93882464insAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.94425677_94425692=	NC_000015.9:g.94425687_94425692del	NC_000015.9:g.94425689_94425692del	NC_000015.9:g.94425690_94425692del	NC_000015.9:g.94425691_94425692del	NC_000015.9:g.94425692del	NC_000015.9:g.94425692dup	NC_000015.9:g.94425691_94425692dup	NC_000015.9:g.94425690_94425692dup	NC_000015.9:g.94425683_94425692dup	NC_000015.9:g.94425692_94425693insAAAAAAAAAAAAAAAAA

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#.

37 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294874207	May 09, 2011 (135)
2	SWEGEN	ss3013784861	Nov 08, 2017 (151)
3	EVA_DECODE	ss3698499218	Jul 13, 2019 (153)
4	EVA_DECODE	ss3698499219	Jul 13, 2019 (153)
5	EVA_DECODE	ss3698499220	Jul 13, 2019 (153)
6	EVA_DECODE	ss3698499221	Jul 13, 2019 (153)
7	EVA_DECODE	ss3698499222	Jul 13, 2019 (153)
8	PACBIO	ss3787933145	Jul 13, 2019 (153)
9	EVA	ss3834387045	Apr 27, 2020 (154)
10	EVA	ss3846286863	Apr 27, 2020 (154)
11	GNOMAD	ss4294106999	Apr 26, 2021 (155)
12	GNOMAD	ss4294107000	Apr 26, 2021 (155)
13	GNOMAD	ss4294107001	Apr 26, 2021 (155)
14	GNOMAD	ss4294107002	Apr 26, 2021 (155)
15	GNOMAD	ss4294107003	Apr 26, 2021 (155)
16	GNOMAD	ss4294107005	Apr 26, 2021 (155)
17	GNOMAD	ss4294107006	Apr 26, 2021 (155)
18	GNOMAD	ss4294107007	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5217630750	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5217630751	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5217630752	Apr 26, 2021 (155)
22	1000G_HIGH_COVERAGE	ss5299524677	Oct 16, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5299524678	Oct 16, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5299524679	Oct 16, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5299524680	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5299524681	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5493128674	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5493128675	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5493128676	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5493128677	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5493128678	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5771871008	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5771871009	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5771871011	Oct 16, 2022 (156)
35	EVA	ss5828619625	Oct 16, 2022 (156)
36	EVA	ss5828619626	Oct 16, 2022 (156)
37	EVA	ss5851418881	Oct 16, 2022 (156)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 478004478 (NC_000015.10:93882447::A 39679/109746) Row 478004479 (NC_000015.10:93882447::AA 160/109976) Row 478004480 (NC_000015.10:93882447::AAA 6/110064)...	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 75600057 (NC_000015.9:94425676::A 4744/16752) Row 75600058 (NC_000015.9:94425676:A: 620/16752) Row 75600059 (NC_000015.9:94425676::AA 11/16752)	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 75600057 (NC_000015.9:94425676::A 4744/16752) Row 75600058 (NC_000015.9:94425676:A: 620/16752) Row 75600059 (NC_000015.9:94425676::AA 11/16752)	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 75600057 (NC_000015.9:94425676::A 4744/16752) Row 75600058 (NC_000015.9:94425676:A: 620/16752) Row 75600059 (NC_000015.9:94425676::AA 11/16752)	-	Apr 26, 2021 (155)
50	14KJPN Submission ignored due to conflicting rows: Row 105708112 (NC_000015.10:93882447:A: 1013/28258) Row 105708113 (NC_000015.10:93882447::A 8279/28258) Row 105708115 (NC_000015.10:93882447::AA 14/28258)	-	Oct 16, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 105708112 (NC_000015.10:93882447:A: 1013/28258) Row 105708113 (NC_000015.10:93882447::A 8279/28258) Row 105708115 (NC_000015.10:93882447::AA 14/28258)	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 105708112 (NC_000015.10:93882447:A: 1013/28258) Row 105708113 (NC_000015.10:93882447::A 8279/28258) Row 105708115 (NC_000015.10:93882447::AA 14/28258)	-	Oct 16, 2022 (156)
53	ALFA	NC_000015.10 - 93882448	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs72431175	May 11, 2012 (137)
rs150674611	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3013784861	NC_000015.9:94425676:AAAA:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3698499222, ss4294107007, ss5299524681, ss5493128678	NC_000015.10:93882447:AAAA:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4294107006	NC_000015.10:93882447:AAA:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4294107005, ss5299524680, ss5493128676	NC_000015.10:93882447:AA:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3698499221	NC_000015.10:93882449:AA:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3787933145, ss3834387045, ss5217630751	NC_000015.9:94425676:A:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5299524678, ss5493128674, ss5771871008, ss5851418881	NC_000015.10:93882447:A:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3698499220	NC_000015.10:93882450:A:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss294874207	NC_000015.8:92226681::A	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5217630750, ss5828619625	NC_000015.9:94425676::A	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3846286863, ss4294106999, ss5299524677, ss5493128675, ss5771871009	NC_000015.10:93882447::A	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3698499219	NC_000015.10:93882451::A	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5217630752, ss5828619626	NC_000015.9:94425676::AA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4294107000, ss5299524679, ss5493128677, ss5771871011	NC_000015.10:93882447::AA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3698499218	NC_000015.10:93882451::AA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4294107001	NC_000015.10:93882447::AAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
141816991	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4294107002	NC_000015.10:93882447::AAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4294107003	NC_000015.10:93882447::AAAAAAAAAAA… NC_000015.10:93882447::AAAAAAAAAAAAAAAAA	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3235701863	NC_000015.10:93882447:AAAAAA:	NC_000015.10:93882447:AAAAAAAAAAAA… NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAA

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

No publications for rs72123421

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

rs72123421