Name: rs67252605
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.

rs67252605

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:73457047-73457056 (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: delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.11118 (1478/13294, ALFA)
delA=0.1719 (774/4502, 1000G)
delA=0.2087 (931/4462, Estonian) (+ 4 more)
delA=0.2709 (1044/3854, ALSPAC)
delA=0.2654 (984/3708, TWINSUK)
delA=0.292 (175/600, NorthernSweden)
delA=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NUMB : 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	13294	AAAAAAAAAA=0.88830	AAAAAAAA=0.00000, AAAAAAAAA=0.11118, AAAAAAAAAAA=0.00053, AAAAAAAAAAAA=0.00000	0.80241	0.024849	0.172741	32
European	Sub	10700	AAAAAAAAAA=0.86290	AAAAAAAA=0.00000, AAAAAAAAA=0.13654, AAAAAAAAAAA=0.00056, AAAAAAAAAAAA=0.00000	0.757111	0.030314	0.212575	28
African	Sub	1806	AAAAAAAAAA=0.9978	AAAAAAAA=0.0000, AAAAAAAAA=0.0022, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000	0.99557	0.0	0.00443	0
African Others	Sub	66	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1740	AAAAAAAAAA=0.9977	AAAAAAAA=0.0000, AAAAAAAAA=0.0023, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000	0.995402	0.0	0.004598	0
Asian	Sub	86	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	70	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	84	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	264	AAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	48	AAAAAAAAAA=0.96	AAAAAAAA=0.00, AAAAAAAAA=0.04, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	0.958333	0.041667	0.0	13
Other	Sub	306	AAAAAAAAAA=0.961	AAAAAAAA=0.000, AAAAAAAAA=0.036, AAAAAAAAAAA=0.003, AAAAAAAAAAAA=0.000	0.940789	0.013158	0.046053	10

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	13294	(A)₁₀=0.88830	delAA=0.00000, delA=0.11118, dupA=0.00053, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	10700	(A)₁₀=0.86290	delAA=0.00000, delA=0.13654, dupA=0.00056, dupAA=0.00000
Allele Frequency Aggregator	African	Sub	1806	(A)₁₀=0.9978	delAA=0.0000, delA=0.0022, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Other	Sub	306	(A)₁₀=0.961	delAA=0.000, delA=0.036, dupA=0.003, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	264	(A)₁₀=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	86	(A)₁₀=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	84	(A)₁₀=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	48	(A)₁₀=0.96	delAA=0.00, delA=0.04, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	4502	(A)₁₀=0.8281	delA=0.1719
1000Genomes	African	Sub	1047	(A)₁₀=0.9847	delA=0.0153
1000Genomes	Europe	Sub	995	(A)₁₀=0.746	delA=0.254
1000Genomes	East Asian	Sub	980	(A)₁₀=0.881	delA=0.119
1000Genomes	South Asian	Sub	802	(A)₁₀=0.732	delA=0.268
1000Genomes	American	Sub	678	(A)₁₀=0.745	delA=0.255
Genetic variation in the Estonian population	Estonian	Study-wide	4462	(A)₁₀=0.7913	delA=0.2087
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₀=0.7291	delA=0.2709
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₀=0.7346	delA=0.2654
Northern Sweden	ACPOP	Study-wide	600	(A)₁₀=0.708	delA=0.292
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₀=0.80	delA=0.20

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 14	NC_000014.9:g.73457055_73457056del
GRCh38.p14 chr 14	NC_000014.9:g.73457056del
GRCh38.p14 chr 14	NC_000014.9:g.73457056dup
GRCh38.p14 chr 14	NC_000014.9:g.73457055_73457056dup
GRCh37.p13 chr 14	NC_000014.8:g.73923762_73923763del
GRCh37.p13 chr 14	NC_000014.8:g.73923763del
GRCh37.p13 chr 14	NC_000014.8:g.73923763dup
GRCh37.p13 chr 14	NC_000014.8:g.73923762_73923763dup
NUMB RefSeqGene	NG_029061.2:g.6533_6534del
NUMB RefSeqGene	NG_029061.2:g.6534del
NUMB RefSeqGene	NG_029061.2:g.6534dup
NUMB RefSeqGene	NG_029061.2:g.6533_6534dup

Gene: NUMB, NUMB endocytic adaptor protein (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NUMB transcript variant 1	NM_001005743.2:c.-233+144… NM_001005743.2:c.-233+1445_-233+1446del	N/A	Intron Variant
NUMB transcript variant 2	NM_001005744.2:c.-233+144… NM_001005744.2:c.-233+1445_-233+1446del	N/A	Intron Variant
NUMB transcript variant 4	NM_001005745.2:c.-233+144… NM_001005745.2:c.-233+1445_-233+1446del	N/A	Intron Variant
NUMB transcript variant 5	NM_001320114.2:c.-148+581… NM_001320114.2:c.-148+581_-148+582del	N/A	Intron Variant
NUMB transcript variant 3	NM_003744.6:c.-233+1445_-… NM_003744.6:c.-233+1445_-233+1446del	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	(A)₁₀=	delAA	delA	dupA	dupAA
GRCh38.p14 chr 14	NC_000014.9:g.73457047_73457056=	NC_000014.9:g.73457055_73457056del	NC_000014.9:g.73457056del	NC_000014.9:g.73457056dup	NC_000014.9:g.73457055_73457056dup
GRCh37.p13 chr 14	NC_000014.8:g.73923754_73923763=	NC_000014.8:g.73923762_73923763del	NC_000014.8:g.73923763del	NC_000014.8:g.73923763dup	NC_000014.8:g.73923762_73923763dup
NUMB RefSeqGene	NG_029061.2:g.6525_6534=	NG_029061.2:g.6533_6534del	NG_029061.2:g.6534del	NG_029061.2:g.6534dup	NG_029061.2:g.6533_6534dup
NUMB transcript variant 1	NM_001005743.1:c.-233+1445=	NM_001005743.1:c.-233+1444_-233+1445del	NM_001005743.1:c.-233+1445del	NM_001005743.1:c.-233+1445dup	NM_001005743.1:c.-233+1444_-233+1445dup
NUMB transcript variant 1	NM_001005743.2:c.-233+1446=	NM_001005743.2:c.-233+1445_-233+1446del	NM_001005743.2:c.-233+1446del	NM_001005743.2:c.-233+1446dup	NM_001005743.2:c.-233+1445_-233+1446dup
NUMB transcript variant 2	NM_001005744.1:c.-233+1445=	NM_001005744.1:c.-233+1444_-233+1445del	NM_001005744.1:c.-233+1445del	NM_001005744.1:c.-233+1445dup	NM_001005744.1:c.-233+1444_-233+1445dup
NUMB transcript variant 2	NM_001005744.2:c.-233+1446=	NM_001005744.2:c.-233+1445_-233+1446del	NM_001005744.2:c.-233+1446del	NM_001005744.2:c.-233+1446dup	NM_001005744.2:c.-233+1445_-233+1446dup
NUMB transcript variant 4	NM_001005745.1:c.-233+1445=	NM_001005745.1:c.-233+1444_-233+1445del	NM_001005745.1:c.-233+1445del	NM_001005745.1:c.-233+1445dup	NM_001005745.1:c.-233+1444_-233+1445dup
NUMB transcript variant 4	NM_001005745.2:c.-233+1446=	NM_001005745.2:c.-233+1445_-233+1446del	NM_001005745.2:c.-233+1446del	NM_001005745.2:c.-233+1446dup	NM_001005745.2:c.-233+1445_-233+1446dup
NUMB transcript variant 5	NM_001320114.2:c.-148+582=	NM_001320114.2:c.-148+581_-148+582del	NM_001320114.2:c.-148+582del	NM_001320114.2:c.-148+582dup	NM_001320114.2:c.-148+581_-148+582dup
NUMB transcript variant 3	NM_003744.5:c.-233+1445=	NM_003744.5:c.-233+1444_-233+1445del	NM_003744.5:c.-233+1445del	NM_003744.5:c.-233+1445dup	NM_003744.5:c.-233+1444_-233+1445dup
NUMB transcript variant 3	NM_003744.6:c.-233+1446=	NM_003744.6:c.-233+1445_-233+1446del	NM_003744.6:c.-233+1446del	NM_003744.6:c.-233+1446dup	NM_003744.6:c.-233+1445_-233+1446dup
NUMB transcript variant X3	XM_005268142.1:c.-148+1445=	XM_005268142.1:c.-148+1444_-148+1445del	XM_005268142.1:c.-148+1445del	XM_005268142.1:c.-148+1445dup	XM_005268142.1:c.-148+1444_-148+1445dup
NUMB transcript variant X5	XM_005268144.1:c.-148+1445=	XM_005268144.1:c.-148+1444_-148+1445del	XM_005268144.1:c.-148+1445del	XM_005268144.1:c.-148+1445dup	XM_005268144.1:c.-148+1444_-148+1445dup
NUMB transcript variant X6	XM_005268145.1:c.-148+1445=	XM_005268145.1:c.-148+1444_-148+1445del	XM_005268145.1:c.-148+1445del	XM_005268145.1:c.-148+1445dup	XM_005268145.1:c.-148+1444_-148+1445dup
NUMB transcript variant X7	XM_005268146.1:c.-148+1445=	XM_005268146.1:c.-148+1444_-148+1445del	XM_005268146.1:c.-148+1445del	XM_005268146.1:c.-148+1445dup	XM_005268146.1:c.-148+1444_-148+1445dup

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#.

51 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95645300	Dec 05, 2013 (138)
2	GMI	ss287920506	May 09, 2011 (137)
3	PJP	ss294838507	May 09, 2011 (134)
4	1000GENOMES	ss327619872	May 09, 2011 (137)
5	1000GENOMES	ss327733242	May 09, 2011 (137)
6	1000GENOMES	ss328140754	Jan 10, 2018 (151)
7	LUNTER	ss552374049	Apr 25, 2013 (138)
8	LUNTER	ss552705973	Apr 25, 2013 (138)
9	LUNTER	ss553554935	Apr 25, 2013 (138)
10	TISHKOFF	ss554744710	Apr 25, 2013 (138)
11	SSMP	ss664242088	Apr 01, 2015 (144)
12	1000GENOMES	ss1374278947	Aug 21, 2014 (142)
13	1000GENOMES	ss1374278951	Aug 21, 2014 (142)
14	EVA_GENOME_DK	ss1574783324	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1708117382	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1708117451	Apr 01, 2015 (144)
17	HAMMER_LAB	ss1807985426	Sep 08, 2015 (146)
18	JJLAB	ss2031238231	Sep 14, 2016 (149)
19	SYSTEMSBIOZJU	ss2628548995	Jan 10, 2018 (151)
20	SWEGEN	ss3012449146	Jan 10, 2018 (151)
21	MCHAISSO	ss3064634607	Jan 10, 2018 (151)
22	BEROUKHIMLAB	ss3644377879	Oct 12, 2018 (152)
23	BIOINF_KMB_FNS_UNIBA	ss3645355611	Oct 12, 2018 (152)
24	URBANLAB	ss3650236740	Oct 12, 2018 (152)
25	EGCUT_WGS	ss3679706036	Jul 13, 2019 (153)
26	EVA_DECODE	ss3696978954	Jul 13, 2019 (153)
27	EVA_DECODE	ss3696978955	Jul 13, 2019 (153)
28	ACPOP	ss3740516531	Jul 13, 2019 (153)
29	PACBIO	ss3787707303	Jul 13, 2019 (153)
30	PACBIO	ss3792738793	Jul 13, 2019 (153)
31	PACBIO	ss3797623127	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3817836420	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3817836421	Jul 13, 2019 (153)
34	EVA	ss3833997760	Apr 27, 2020 (154)
35	EVA	ss3840590048	Apr 27, 2020 (154)
36	EVA	ss3846079628	Apr 27, 2020 (154)
37	GNOMAD	ss4280670153	Apr 26, 2021 (155)
38	GNOMAD	ss4280670154	Apr 26, 2021 (155)
39	GNOMAD	ss4280670155	Apr 26, 2021 (155)
40	TOPMED	ss4975906588	Apr 26, 2021 (155)
41	TOPMED	ss4975906589	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5213917800	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5213917801	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5296754194	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5296754195	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5490746564	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5490746565	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5766919687	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5766919688	Oct 16, 2022 (156)
50	EVA	ss5841319757	Oct 16, 2022 (156)
51	EVA	ss5947968919	Oct 16, 2022 (156)
52	1000Genomes	NC_000014.8 - 73923754	Oct 12, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children	NC_000014.8 - 73923754	Oct 12, 2018 (152)
54	Genetic variation in the Estonian population	NC_000014.8 - 73923754	Oct 12, 2018 (152)
55	The Danish reference pan genome	NC_000014.8 - 73923754	Apr 27, 2020 (154)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455570479 (NC_000014.9:73457046::A 7957/136930) Row 455570480 (NC_000014.9:73457046::AA 1/136996) Row 455570481 (NC_000014.9:73457046:A: 24861/136936)	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455570479 (NC_000014.9:73457046::A 7957/136930) Row 455570480 (NC_000014.9:73457046::AA 1/136996) Row 455570481 (NC_000014.9:73457046:A: 24861/136936)	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455570479 (NC_000014.9:73457046::A 7957/136930) Row 455570480 (NC_000014.9:73457046::AA 1/136996) Row 455570481 (NC_000014.9:73457046:A: 24861/136936)	-	Apr 26, 2021 (155)
59	Northern Sweden	NC_000014.8 - 73923754	Jul 13, 2019 (153)
60	8.3KJPN Submission ignored due to conflicting rows: Row 71887107 (NC_000014.8:73923753::A 639/16760) Row 71887108 (NC_000014.8:73923753:A: 1714/16760)	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 71887107 (NC_000014.8:73923753::A 639/16760) Row 71887108 (NC_000014.8:73923753:A: 1714/16760)	-	Apr 26, 2021 (155)
62	14KJPN Submission ignored due to conflicting rows: Row 100756791 (NC_000014.9:73457046:A: 2846/28258) Row 100756792 (NC_000014.9:73457046::A 1150/28258)	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 100756791 (NC_000014.9:73457046:A: 2846/28258) Row 100756792 (NC_000014.9:73457046::A 1150/28258)	-	Oct 16, 2022 (156)
64	TopMed Submission ignored due to conflicting rows: Row 191452247 (NC_000014.9:73457046:A: 48333/264690) Row 191452248 (NC_000014.9:73457046:AA: 4/264690)	-	Apr 26, 2021 (155)
65	TopMed Submission ignored due to conflicting rows: Row 191452247 (NC_000014.9:73457046:A: 48333/264690) Row 191452248 (NC_000014.9:73457046:AA: 4/264690)	-	Apr 26, 2021 (155)
66	UK 10K study - Twins	NC_000014.8 - 73923754	Oct 12, 2018 (152)
67	ALFA	NC_000014.9 - 73457047	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)
rs67252606	Feb 26, 2009 (130)
rs147526963	May 11, 2012 (137)
rs148475320	May 04, 2012 (137)
rs369716794	May 13, 2013 (138)
rs373058978	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4975906589	NC_000014.9:73457046:AA:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAA	(self)
7760158492	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAA	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAA	(self)
ss327619872, ss327733242, ss552374049, ss553554935	NC_000014.7:72993506:A:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
ss294838507	NC_000014.7:72993515:A:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
64612983, 35905171, 25444284, 460453, 13801396, 35905171, ss664242088, ss1374278947, ss1574783324, ss1708117382, ss1708117451, ss2031238231, ss2628548995, ss3012449146, ss3644377879, ss3679706036, ss3740516531, ss3787707303, ss3792738793, ss3797623127, ss3840590048, ss5213917801, ss5841319757, ss5947968919	NC_000014.8:73923753:A:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
ss554744710	NC_000014.8:73923762:A:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
ss3064634607, ss3645355611, ss3650236740, ss3696978955, ss3817836421, ss3846079628, ss4280670155, ss4975906588, ss5296754195, ss5490746564, ss5766919687	NC_000014.9:73457046:A:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
7760158492	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
ss287920506	NT_026437.12:54923753:A:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
ss95645300	NT_026437.12:54923762:A:	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA	(self)
ss328140754, ss552705973	NC_000014.7:72993506::A	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss1807985426, ss3833997760, ss5213917800	NC_000014.8:73923753::A	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss1374278951	NC_000014.8:73923754::A	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss4280670153, ss5296754194, ss5490746565, ss5766919688	NC_000014.9:73457046::A	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA	(self)
7760158492	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3696978954, ss3817836420	NC_000014.9:73457047::A	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss4280670154	NC_000014.9:73457046::AA	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAAA	(self)
7760158492	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAAA	NC_000014.9:73457046:AAAAAAAAAA:AA… NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAAA	(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 rs67252605

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

rs67252605