Name: rs11322033
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.

rs11322033

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr21:14378625-14378637 (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(T)₇ / delTT / delT / dupT / du…
del(T)₇ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.07080 (776/10960, ALFA)
dupTT=0.2071 (798/3854, ALSPAC)
dupTT=0.2077 (770/3708, TWINSUK) (+ 2 more)
(T)₁₃=0.3986 (570/1430, 1000G)
dupTT=0.30 (12/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HSPA13 : 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	10960	TTTTTTTTTTTTT=0.91524	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.01396, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.07080, TTTTTTTTTTTTTTTT=0.00000	0.877696	0.018195	0.104108	32
European	Sub	8894	TTTTTTTTTTTTT=0.8955	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0172, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0872, TTTTTTTTTTTTTTTT=0.0000	0.848302	0.022569	0.12913	32
African	Sub	1142	TTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	38	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1104	TTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	68	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	62	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	94	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	442	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	262	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	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	10960	(T)₁₃=0.91524	delTT=0.00000, delT=0.01396, dupT=0.00000, dupTT=0.07080, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	8894	(T)₁₃=0.8955	delTT=0.0000, delT=0.0172, dupT=0.0000, dupTT=0.0872, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	1142	(T)₁₃=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	442	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	262	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	94	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	68	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupTT=0.2071
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupTT=0.2077
1000Genomes	Global	Study-wide	1430	(T)₁₃=0.3986	delT=0.6014
1000Genomes	African	Sub	529	(T)₁₃=0.147	delT=0.853
1000Genomes	East Asian	Sub	268	(T)₁₃=0.429	delT=0.571
1000Genomes	Europe	Sub	266	(T)₁₃=0.680	delT=0.320
1000Genomes	South Asian	Sub	225	(T)₁₃=0.604	delT=0.396
1000Genomes	American	Sub	142	(T)₁₃=0.423	delT=0.577
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupTT=0.30

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 21	NC_000021.9:g.14378631_14378637del
GRCh38.p14 chr 21	NC_000021.9:g.14378636_14378637del
GRCh38.p14 chr 21	NC_000021.9:g.14378637del
GRCh38.p14 chr 21	NC_000021.9:g.14378637dup
GRCh38.p14 chr 21	NC_000021.9:g.14378636_14378637dup
GRCh38.p14 chr 21	NC_000021.9:g.14378635_14378637dup
GRCh38.p14 chr 21	NC_000021.9:g.14378634_14378637dup
GRCh38.p14 chr 21	NC_000021.9:g.14378627_14378637dup
GRCh37.p13 chr 21	NC_000021.8:g.15750952_15750958del
GRCh37.p13 chr 21	NC_000021.8:g.15750957_15750958del
GRCh37.p13 chr 21	NC_000021.8:g.15750958del
GRCh37.p13 chr 21	NC_000021.8:g.15750958dup
GRCh37.p13 chr 21	NC_000021.8:g.15750957_15750958dup
GRCh37.p13 chr 21	NC_000021.8:g.15750956_15750958dup
GRCh37.p13 chr 21	NC_000021.8:g.15750955_15750958dup
GRCh37.p13 chr 21	NC_000021.8:g.15750948_15750958dup

Gene: HSPA13, heat shock protein family A (Hsp70) member 13 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HSPA13 transcript	NM_006948.5:c.367-219_367… NM_006948.5:c.367-219_367-213del	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	(T)₁₃=	del(T)₇	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₁₁
GRCh38.p14 chr 21	NC_000021.9:g.14378625_14378637=	NC_000021.9:g.14378631_14378637del	NC_000021.9:g.14378636_14378637del	NC_000021.9:g.14378637del	NC_000021.9:g.14378637dup	NC_000021.9:g.14378636_14378637dup	NC_000021.9:g.14378635_14378637dup	NC_000021.9:g.14378634_14378637dup	NC_000021.9:g.14378627_14378637dup
GRCh37.p13 chr 21	NC_000021.8:g.15750946_15750958=	NC_000021.8:g.15750952_15750958del	NC_000021.8:g.15750957_15750958del	NC_000021.8:g.15750958del	NC_000021.8:g.15750958dup	NC_000021.8:g.15750957_15750958dup	NC_000021.8:g.15750956_15750958dup	NC_000021.8:g.15750955_15750958dup	NC_000021.8:g.15750948_15750958dup
HSPA13 transcript	NM_006948.4:c.367-213=	NM_006948.4:c.367-219_367-213del	NM_006948.4:c.367-214_367-213del	NM_006948.4:c.367-213del	NM_006948.4:c.367-213dup	NM_006948.4:c.367-214_367-213dup	NM_006948.4:c.367-215_367-213dup	NM_006948.4:c.367-216_367-213dup	NM_006948.4:c.367-223_367-213dup
HSPA13 transcript	NM_006948.5:c.367-213=	NM_006948.5:c.367-219_367-213del	NM_006948.5:c.367-214_367-213del	NM_006948.5:c.367-213del	NM_006948.5:c.367-213dup	NM_006948.5:c.367-214_367-213dup	NM_006948.5:c.367-215_367-213dup	NM_006948.5:c.367-216_367-213dup	NM_006948.5:c.367-223_367-213dup
HSPA13 transcript variant X1	XM_005261036.1:c.-45+2578=	XM_005261036.1:c.-45+2572_-45+2578del	XM_005261036.1:c.-45+2577_-45+2578del	XM_005261036.1:c.-45+2578del	XM_005261036.1:c.-45+2578dup	XM_005261036.1:c.-45+2577_-45+2578dup	XM_005261036.1:c.-45+2576_-45+2578dup	XM_005261036.1:c.-45+2575_-45+2578dup	XM_005261036.1:c.-45+2568_-45+2578dup

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#.

52 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss289423136	May 04, 2012 (137)
2	SSMP	ss664493207	Apr 01, 2015 (144)
3	SSIP	ss947408201	Aug 21, 2014 (142)
4	1000GENOMES	ss1378643411	Aug 21, 2014 (142)
5	1000GENOMES	ss1378643412	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1575746535	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1709432836	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1709433416	Apr 01, 2015 (144)
9	HAMMER_LAB	ss1809597781	Sep 08, 2015 (146)
10	SWEGEN	ss3018606164	Nov 08, 2017 (151)
11	MCHAISSO	ss3065831407	Nov 08, 2017 (151)
12	EVA_DECODE	ss3707380932	Jul 13, 2019 (153)
13	EVA_DECODE	ss3707380933	Jul 13, 2019 (153)
14	EVA_DECODE	ss3707380934	Jul 13, 2019 (153)
15	EVA_DECODE	ss3707380935	Jul 13, 2019 (153)
16	EVA_DECODE	ss3707380936	Jul 13, 2019 (153)
17	ACPOP	ss3743571064	Jul 13, 2019 (153)
18	ACPOP	ss3743571065	Jul 13, 2019 (153)
19	PACBIO	ss3788712072	Jul 13, 2019 (153)
20	PACBIO	ss3788712073	Jul 13, 2019 (153)
21	PACBIO	ss3793592973	Jul 13, 2019 (153)
22	PACBIO	ss3793592974	Jul 13, 2019 (153)
23	PACBIO	ss3798479103	Jul 13, 2019 (153)
24	PACBIO	ss3798479104	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3822049767	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3822049768	Jul 13, 2019 (153)
27	EVA	ss3835775839	Apr 27, 2020 (154)
28	GNOMAD	ss4357362632	Apr 26, 2021 (155)
29	GNOMAD	ss4357362633	Apr 26, 2021 (155)
30	GNOMAD	ss4357362634	Apr 26, 2021 (155)
31	GNOMAD	ss4357362635	Apr 26, 2021 (155)
32	GNOMAD	ss4357362636	Apr 26, 2021 (155)
33	GNOMAD	ss4357362637	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5230751753	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5230751754	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5230751755	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5230751756	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5309598283	Oct 13, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5309598284	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5309598285	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5501701999	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5501702000	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5501702001	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5501702002	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5791051178	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5791051179	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5791051180	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5791051181	Oct 13, 2022 (156)
49	EVA	ss5838799093	Oct 13, 2022 (156)
50	EVA	ss5838799094	Oct 13, 2022 (156)
51	EVA	ss5958533522	Oct 13, 2022 (156)
52	EVA	ss5981105070	Oct 13, 2022 (156)
53	1000Genomes	NC_000021.8 - 15750946	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children	NC_000021.8 - 15750946	Oct 12, 2018 (152)
55	The Danish reference pan genome	NC_000021.8 - 15750946	Apr 27, 2020 (154)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227911 (NC_000021.9:14378624::T 307/133858) Row 558227912 (NC_000021.9:14378624::TT 20857/133816) Row 558227913 (NC_000021.9:14378624::TTT 25/133934)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227911 (NC_000021.9:14378624::T 307/133858) Row 558227912 (NC_000021.9:14378624::TT 20857/133816) Row 558227913 (NC_000021.9:14378624::TTT 25/133934)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227911 (NC_000021.9:14378624::T 307/133858) Row 558227912 (NC_000021.9:14378624::TT 20857/133816) Row 558227913 (NC_000021.9:14378624::TTT 25/133934)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227911 (NC_000021.9:14378624::T 307/133858) Row 558227912 (NC_000021.9:14378624::TT 20857/133816) Row 558227913 (NC_000021.9:14378624::TTT 25/133934)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227911 (NC_000021.9:14378624::T 307/133858) Row 558227912 (NC_000021.9:14378624::TT 20857/133816) Row 558227913 (NC_000021.9:14378624::TTT 25/133934)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227911 (NC_000021.9:14378624::T 307/133858) Row 558227912 (NC_000021.9:14378624::TT 20857/133816) Row 558227913 (NC_000021.9:14378624::TTT 25/133934)...	-	Apr 26, 2021 (155)
62	Northern Sweden Submission ignored due to conflicting rows: Row 16855929 (NC_000021.8:15750945::TT 113/598) Row 16855930 (NC_000021.8:15750945:T: 24/598)	-	Jul 13, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 16855929 (NC_000021.8:15750945::TT 113/598) Row 16855930 (NC_000021.8:15750945:T: 24/598)	-	Jul 13, 2019 (153)
64	8.3KJPN Submission ignored due to conflicting rows: Row 88721060 (NC_000021.8:15750945:T: 1259/16760) Row 88721061 (NC_000021.8:15750945::TT 1555/16760) Row 88721062 (NC_000021.8:15750945::TTT 10/16760)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 88721060 (NC_000021.8:15750945:T: 1259/16760) Row 88721061 (NC_000021.8:15750945::TT 1555/16760) Row 88721062 (NC_000021.8:15750945::TTT 10/16760)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 88721060 (NC_000021.8:15750945:T: 1259/16760) Row 88721061 (NC_000021.8:15750945::TT 1555/16760) Row 88721062 (NC_000021.8:15750945::TTT 10/16760)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 88721060 (NC_000021.8:15750945:T: 1259/16760) Row 88721061 (NC_000021.8:15750945::TT 1555/16760) Row 88721062 (NC_000021.8:15750945::TTT 10/16760)...	-	Apr 26, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 124888282 (NC_000021.9:14378624::TT 2689/28258) Row 124888283 (NC_000021.9:14378624:T: 2029/28258) Row 124888284 (NC_000021.9:14378624::TTT 13/28258)...	-	Oct 13, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 124888282 (NC_000021.9:14378624::TT 2689/28258) Row 124888283 (NC_000021.9:14378624:T: 2029/28258) Row 124888284 (NC_000021.9:14378624::TTT 13/28258)...	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 124888282 (NC_000021.9:14378624::TT 2689/28258) Row 124888283 (NC_000021.9:14378624:T: 2029/28258) Row 124888284 (NC_000021.9:14378624::TTT 13/28258)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 124888282 (NC_000021.9:14378624::TT 2689/28258) Row 124888283 (NC_000021.9:14378624:T: 2029/28258) Row 124888284 (NC_000021.9:14378624::TTT 13/28258)...	-	Oct 13, 2022 (156)
72	UK 10K study - Twins	NC_000021.8 - 15750946	Oct 12, 2018 (152)
73	ALFA	NC_000021.9 - 14378625	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
ss5501702002	NC_000021.9:14378624:TTTTTTT:	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTT
ss4357362637	NC_000021.9:14378624:TT:	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
6881307131	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss289423136	NC_000021.7:14672816:T:	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
79077240, ss1378643411, ss1809597781, ss3018606164, ss3743571065, ss3835775839, ss5230751753	NC_000021.8:15750945:T:	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3065831407, ss3707380932, ss3822049768, ss4357362636, ss5309598284, ss5501701999, ss5791051179	NC_000021.9:14378624:T:	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
6881307131	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3788712073, ss3793592973, ss3798479103, ss5230751756	NC_000021.8:15750945::T	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4357362632, ss5309598285, ss5501702001, ss5791051181	NC_000021.9:14378624::T	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6881307131	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3707380933	NC_000021.9:14378625::T	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
43755644, 770044, 43755644, ss664493207, ss947408201, ss1575746535, ss1709432836, ss1709433416, ss3743571064, ss3788712072, ss3793592974, ss3798479104, ss5230751754, ss5838799093, ss5958533522, ss5981105070	NC_000021.8:15750945::TT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1378643412	NC_000021.8:15750946::TT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4357362633, ss5309598283, ss5501702000, ss5791051178	NC_000021.9:14378624::TT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6881307131	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3707380934, ss3822049767	NC_000021.9:14378625::TT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5230751755, ss5838799094	NC_000021.8:15750945::TTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4357362634, ss5791051180	NC_000021.9:14378624::TTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6881307131	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3707380935	NC_000021.9:14378625::TTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4357362635	NC_000021.9:14378624::TTTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3707380936	NC_000021.9:14378625::TTTTTTTTTTT	NC_000021.9:14378624:TTTTTTTTTTTTT… NC_000021.9:14378624:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(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 rs11322033

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

rs11322033