Name: rs71328849
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.

rs71328849

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:30405069-30405079 (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=0.000008 (2/264690, TOPMED)
dupA=0.03740 (525/14038, ALFA)
dupA=0.1625 (814/5008, 1000G) (+ 5 more)
dupA=0.2216 (854/3854, ALSPAC)
dupA=0.2087 (774/3708, TWINSUK)
dupA=0.249 (249/998, GoNL)
dupA=0.164 (98/596, NorthernSweden)
dupA=0.05 (2/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SEC14L2 : 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	14038	AAAAAAAAAAA=0.96253	AAAAAAAA=0.00000, AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.03740, AAAAAAAAAAAAA=0.00007	0.930892	0.0057	0.063408	32
European	Sub	10932	AAAAAAAAAAA=0.95207	AAAAAAAA=0.00000, AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.04784, AAAAAAAAAAAAA=0.00009	0.911619	0.007319	0.081061	34
African	Sub	2124	AAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	90	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	2034	AAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	88	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	66	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	88	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	418	AAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	72	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	316	AAAAAAAAAAA=0.994	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.006, AAAAAAAAAAAAA=0.000	0.987342	0.0	0.012658	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
TopMed	Global	Study-wide	264690	(A)₁₁=0.999992	delAAA=0.000008
Allele Frequency Aggregator	Total	Global	14038	(A)₁₁=0.96253	delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.03740, dupAA=0.00007
Allele Frequency Aggregator	European	Sub	10932	(A)₁₁=0.95207	delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.04784, dupAA=0.00009
Allele Frequency Aggregator	African	Sub	2124	(A)₁₁=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	418	(A)₁₁=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	316	(A)₁₁=0.994	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.006, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	88	(A)₁₁=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	88	(A)₁₁=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	72	(A)₁₁=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.1625
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.1596
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.1548
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.2435
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.097
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.154
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupA=0.2216
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupA=0.2087
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupA=0.249
Northern Sweden	ACPOP	Study-wide	596	- No frequency provided	dupA=0.164
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.05

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 22	NC_000022.11:g.30405077_30405079del
GRCh38.p14 chr 22	NC_000022.11:g.30405078_30405079del
GRCh38.p14 chr 22	NC_000022.11:g.30405079del
GRCh38.p14 chr 22	NC_000022.11:g.30405079dup
GRCh38.p14 chr 22	NC_000022.11:g.30405078_30405079dup
GRCh37.p13 chr 22	NC_000022.10:g.30801066_30801068del
GRCh37.p13 chr 22	NC_000022.10:g.30801067_30801068del
GRCh37.p13 chr 22	NC_000022.10:g.30801068del
GRCh37.p13 chr 22	NC_000022.10:g.30801068dup
GRCh37.p13 chr 22	NC_000022.10:g.30801067_30801068dup

Gene: SEC14L2, SEC14 like lipid binding 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SEC14L2 transcript variant 3	NM_001204204.3:c.131-1265… NM_001204204.3:c.131-1265_131-1263del	N/A	Intron Variant
SEC14L2 transcript variant 4	NM_001291932.2:c.-32-1265… NM_001291932.2:c.-32-1265_-32-1263del	N/A	Intron Variant
SEC14L2 transcript variant 1	NM_012429.5:c.131-1265_13… NM_012429.5:c.131-1265_131-1263del	N/A	Intron Variant
SEC14L2 transcript variant 2	NM_033382.3:c.131-1265_13… NM_033382.3:c.131-1265_131-1263del	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)₁₁=	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 22	NC_000022.11:g.30405069_30405079=	NC_000022.11:g.30405077_30405079del	NC_000022.11:g.30405078_30405079del	NC_000022.11:g.30405079del	NC_000022.11:g.30405079dup	NC_000022.11:g.30405078_30405079dup
GRCh37.p13 chr 22	NC_000022.10:g.30801058_30801068=	NC_000022.10:g.30801066_30801068del	NC_000022.10:g.30801067_30801068del	NC_000022.10:g.30801068del	NC_000022.10:g.30801068dup	NC_000022.10:g.30801067_30801068dup
SEC14L2 transcript variant 3	NM_001204204.1:c.131-1273=	NM_001204204.1:c.131-1265_131-1263del	NM_001204204.1:c.131-1264_131-1263del	NM_001204204.1:c.131-1263del	NM_001204204.1:c.131-1263dup	NM_001204204.1:c.131-1264_131-1263dup
SEC14L2 transcript variant 3	NM_001204204.3:c.131-1273=	NM_001204204.3:c.131-1265_131-1263del	NM_001204204.3:c.131-1264_131-1263del	NM_001204204.3:c.131-1263del	NM_001204204.3:c.131-1263dup	NM_001204204.3:c.131-1264_131-1263dup
SEC14L2 transcript variant 4	NM_001291932.2:c.-32-1273=	NM_001291932.2:c.-32-1265_-32-1263del	NM_001291932.2:c.-32-1264_-32-1263del	NM_001291932.2:c.-32-1263del	NM_001291932.2:c.-32-1263dup	NM_001291932.2:c.-32-1264_-32-1263dup
SEC14L2 transcript variant 1	NM_012429.3:c.131-1273=	NM_012429.3:c.131-1265_131-1263del	NM_012429.3:c.131-1264_131-1263del	NM_012429.3:c.131-1263del	NM_012429.3:c.131-1263dup	NM_012429.3:c.131-1264_131-1263dup
SEC14L2 transcript variant 1	NM_012429.5:c.131-1273=	NM_012429.5:c.131-1265_131-1263del	NM_012429.5:c.131-1264_131-1263del	NM_012429.5:c.131-1263del	NM_012429.5:c.131-1263dup	NM_012429.5:c.131-1264_131-1263dup
SEC14L2 transcript variant 2	NM_033382.2:c.131-1273=	NM_033382.2:c.131-1265_131-1263del	NM_033382.2:c.131-1264_131-1263del	NM_033382.2:c.131-1263del	NM_033382.2:c.131-1263dup	NM_033382.2:c.131-1264_131-1263dup
SEC14L2 transcript variant 2	NM_033382.3:c.131-1273=	NM_033382.3:c.131-1265_131-1263del	NM_033382.3:c.131-1264_131-1263del	NM_033382.3:c.131-1263del	NM_033382.3:c.131-1263dup	NM_033382.3:c.131-1264_131-1263dup
SEC14L2 transcript variant X1	XM_005261425.1:c.-32-1273=	XM_005261425.1:c.-32-1265_-32-1263del	XM_005261425.1:c.-32-1264_-32-1263del	XM_005261425.1:c.-32-1263del	XM_005261425.1:c.-32-1263dup	XM_005261425.1:c.-32-1264_-32-1263dup
SEC14L2 transcript variant X2	XM_005261426.1:c.-32-1273=	XM_005261426.1:c.-32-1265_-32-1263del	XM_005261426.1:c.-32-1264_-32-1263del	XM_005261426.1:c.-32-1263del	XM_005261426.1:c.-32-1263dup	XM_005261426.1:c.-32-1264_-32-1263dup
SEC14L2 transcript variant X3	XM_005261427.1:c.131-1273=	XM_005261427.1:c.131-1265_131-1263del	XM_005261427.1:c.131-1264_131-1263del	XM_005261427.1:c.131-1263del	XM_005261427.1:c.131-1263dup	XM_005261427.1:c.131-1264_131-1263dup

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#.

44 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss96109804	Feb 13, 2009 (130)
2	GMI	ss289445565	May 04, 2012 (138)
3	1000GENOMES	ss499857116	May 04, 2012 (137)
4	TISHKOFF	ss566460195	Apr 25, 2013 (138)
5	SSMP	ss664522310	Apr 01, 2015 (144)
6	EVA-GONL	ss995304193	Aug 21, 2014 (142)
7	1000GENOMES	ss1378982682	Aug 21, 2014 (142)
8	EVA_GENOME_DK	ss1575823890	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709571596	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1709571625	Apr 01, 2015 (144)
11	JJLAB	ss2031465695	Sep 14, 2016 (149)
12	SYSTEMSBIOZJU	ss2629602135	Nov 08, 2017 (151)
13	SWEGEN	ss3019230836	Nov 08, 2017 (151)
14	MCHAISSO	ss3064885240	Nov 08, 2017 (151)
15	BEROUKHIMLAB	ss3644459456	Oct 12, 2018 (152)
16	BIOINF_KMB_FNS_UNIBA	ss3645681697	Oct 12, 2018 (152)
17	ILLUMINA	ss3654004745	Oct 12, 2018 (152)
18	EVA_DECODE	ss3708110412	Jul 13, 2019 (153)
19	EVA_DECODE	ss3708110413	Jul 13, 2019 (153)
20	ACPOP	ss3743893463	Jul 13, 2019 (153)
21	PACBIO	ss3788816244	Jul 13, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3822492446	Jul 13, 2019 (153)
23	EVA	ss3835967858	Apr 27, 2020 (154)
24	EVA	ss3841612197	Apr 27, 2020 (154)
25	EVA	ss3847127031	Apr 27, 2020 (154)
26	GNOMAD	ss4363864485	Apr 26, 2021 (155)
27	GNOMAD	ss4363864486	Apr 26, 2021 (155)
28	GNOMAD	ss4363864487	Apr 26, 2021 (155)
29	GNOMAD	ss4363864488	Apr 26, 2021 (155)
30	TOPMED	ss5107721224	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5232426661	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5232426662	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5232426663	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5310947449	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5502803460	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5502803461	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5793484620	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5793484621	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5793484622	Oct 16, 2022 (156)
40	YY_MCH	ss5818674014	Oct 16, 2022 (156)
41	EVA	ss5822010425	Oct 16, 2022 (156)
42	EVA	ss5853376981	Oct 16, 2022 (156)
43	EVA	ss5881648338	Oct 16, 2022 (156)
44	EVA	ss5959260981	Oct 16, 2022 (156)
45	1000Genomes	NC_000022.10 - 30801058	Oct 12, 2018 (152)
46	The Avon Longitudinal Study of Parents and Children	NC_000022.10 - 30801058	Oct 12, 2018 (152)
47	The Danish reference pan genome	NC_000022.10 - 30801058	Apr 27, 2020 (154)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 568738613 (NC_000022.11:30405068::A 26756/127426) Row 568738614 (NC_000022.11:30405068::AA 17/127646) Row 568738615 (NC_000022.11:30405068:A: 32/127516)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 568738613 (NC_000022.11:30405068::A 26756/127426) Row 568738614 (NC_000022.11:30405068::AA 17/127646) Row 568738615 (NC_000022.11:30405068:A: 32/127516)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 568738613 (NC_000022.11:30405068::A 26756/127426) Row 568738614 (NC_000022.11:30405068::AA 17/127646) Row 568738615 (NC_000022.11:30405068:A: 32/127516)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 568738613 (NC_000022.11:30405068::A 26756/127426) Row 568738614 (NC_000022.11:30405068::AA 17/127646) Row 568738615 (NC_000022.11:30405068:A: 32/127516)...	-	Apr 26, 2021 (155)
52	Genome of the Netherlands Release 5	NC_000022.10 - 30801058	Apr 27, 2020 (154)
53	Northern Sweden	NC_000022.10 - 30801058	Jul 13, 2019 (153)
54	8.3KJPN Submission ignored due to conflicting rows: Row 90395968 (NC_000022.10:30801057::A 1362/16760) Row 90395969 (NC_000022.10:30801057:A: 17/16760) Row 90395970 (NC_000022.10:30801057::AA 5/16760)	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 90395968 (NC_000022.10:30801057::A 1362/16760) Row 90395969 (NC_000022.10:30801057:A: 17/16760) Row 90395970 (NC_000022.10:30801057::AA 5/16760)	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 90395968 (NC_000022.10:30801057::A 1362/16760) Row 90395969 (NC_000022.10:30801057:A: 17/16760) Row 90395970 (NC_000022.10:30801057::AA 5/16760)	-	Apr 26, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 127321724 (NC_000022.11:30405068::A 2223/28256) Row 127321725 (NC_000022.11:30405068::AA 7/28256) Row 127321726 (NC_000022.11:30405068:A: 15/28256)	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 127321724 (NC_000022.11:30405068::A 2223/28256) Row 127321725 (NC_000022.11:30405068::AA 7/28256) Row 127321726 (NC_000022.11:30405068:A: 15/28256)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 127321724 (NC_000022.11:30405068::A 2223/28256) Row 127321725 (NC_000022.11:30405068::AA 7/28256) Row 127321726 (NC_000022.11:30405068:A: 15/28256)	-	Oct 16, 2022 (156)
60	TopMed	NC_000022.11 - 30405069	Apr 26, 2021 (155)
61	UK 10K study - Twins	NC_000022.10 - 30801058	Oct 12, 2018 (152)
62	ALFA	NC_000022.11 - 30405069	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)
rs200409784	May 15, 2013 (138)
rs369739542	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
382830171, ss5107721224	NC_000022.11:30405068:AAA:	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAA	(self)
9079844383	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAA	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAA	(self)
ss4363864488	NC_000022.11:30405068:AA:	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAA	(self)
9079844383	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAA	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAA	(self)
ss3788816244, ss5232426662	NC_000022.10:30801057:A:	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss3708110413, ss4363864487, ss5793484622	NC_000022.11:30405068:A:	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAA	(self)
9079844383	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAA	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss289445565	NC_000022.9:29131068::A	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
80538581, 44546362, 792756, 19850438, 17178328, 44546362, ss499857116, ss664522310, ss995304193, ss1378982682, ss1575823890, ss1709571596, ss1709571625, ss2031465695, ss2629602135, ss3019230836, ss3644459456, ss3654004745, ss3743893463, ss3835967858, ss3841612197, ss5232426661, ss5822010425, ss5959260981	NC_000022.10:30801057::A	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss566460195	NC_000022.10:30801068::A	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3064885240, ss3645681697, ss3822492446, ss3847127031, ss4363864485, ss5310947449, ss5502803460, ss5793484620, ss5818674014, ss5853376981, ss5881648338	NC_000022.11:30405068::A	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
9079844383	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3708110412	NC_000022.11:30405069::A	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss96109804	NT_011520.12:10191626::A	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5232426663	NC_000022.10:30801057::AA	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4363864486, ss5502803461, ss5793484621	NC_000022.11:30405068::AA	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9079844383	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAAA	NC_000022.11:30405068:AAAAAAAAAAA:… NC_000022.11:30405068:AAAAAAAAAAA:AAAAAAAAAAAAA	(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 rs71328849

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

rs71328849