Name: rs33966783
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.

rs33966783

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:29686301-29686318 (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)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.0501 (461/9210, ALFA)
delT=0.3207 (1606/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DPY19L2P3 : Intron Variant
ZNRF2P2 : 2KB Upstream Variant
LOC646762 : 2KB Upstream 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	9210	TTTTTTTTTTTTTTTTTT=0.9111	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0377, TTTTTTTTTTTTTTTTT=0.0501, TTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.911392	0.007736	0.080872	32
European	Sub	7850	TTTTTTTTTTTTTTTTTT=0.8959	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0442, TTTTTTTTTTTTTTTTT=0.0585, TTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.895148	0.009202	0.09565	24
African	Sub	644	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	622	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	96	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	78	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	68	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	286	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	72	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	194	TTTTTTTTTTTTTTTTTT=0.990	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.010, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	0.979381	0.0	0.020619	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9210	(T)₁₈=0.9111	delTTT=0.0000, delTT=0.0377, delT=0.0501, dupT=0.0012, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	7850	(T)₁₈=0.8959	delTTT=0.0000, delTT=0.0442, delT=0.0585, dupT=0.0014, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	644	(T)₁₈=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	286	(T)₁₈=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	194	(T)₁₈=0.990	delTTT=0.000, delTT=0.000, delT=0.010, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	96	(T)₁₈=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	72	(T)₁₈=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	68	(T)₁₈=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₈=0.6793	delT=0.3207
1000Genomes	African	Sub	1322	(T)₁₈=0.5303	delT=0.4697
1000Genomes	East Asian	Sub	1008	(T)₁₈=0.8730	delT=0.1270
1000Genomes	Europe	Sub	1006	(T)₁₈=0.6412	delT=0.3588
1000Genomes	South Asian	Sub	978	(T)₁₈=0.764	delT=0.236
1000Genomes	American	Sub	694	(T)₁₈=0.618	delT=0.382

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 7	NC_000007.14:g.29686314_29686318del
GRCh38.p14 chr 7	NC_000007.14:g.29686315_29686318del
GRCh38.p14 chr 7	NC_000007.14:g.29686316_29686318del
GRCh38.p14 chr 7	NC_000007.14:g.29686317_29686318del
GRCh38.p14 chr 7	NC_000007.14:g.29686318del
GRCh38.p14 chr 7	NC_000007.14:g.29686318dup
GRCh38.p14 chr 7	NC_000007.14:g.29686317_29686318dup
GRCh38.p14 chr 7	NC_000007.14:g.29686316_29686318dup
GRCh38.p14 chr 7	NC_000007.14:g.29686310_29686318dup
GRCh37.p13 chr 7	NC_000007.13:g.29725930_29725934del
GRCh37.p13 chr 7	NC_000007.13:g.29725931_29725934del
GRCh37.p13 chr 7	NC_000007.13:g.29725932_29725934del
GRCh37.p13 chr 7	NC_000007.13:g.29725933_29725934del
GRCh37.p13 chr 7	NC_000007.13:g.29725934del
GRCh37.p13 chr 7	NC_000007.13:g.29725934dup
GRCh37.p13 chr 7	NC_000007.13:g.29725933_29725934dup
GRCh37.p13 chr 7	NC_000007.13:g.29725932_29725934dup
GRCh37.p13 chr 7	NC_000007.13:g.29725926_29725934dup

Gene: DPY19L2P3, DPY19L2 pseudogene 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DPY19L2P3 transcript variant 2	NR_036482.1:n.	N/A	Intron Variant
DPY19L2P3 transcript variant 3	NR_158194.1:n.	N/A	Intron Variant

Gene: LOC646762, uncharacterized LOC646762 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
MIR550A3HG transcript	NR_024278.1:n.	N/A	Upstream Transcript Variant

Gene: ZNRF2P2, zinc and ring finger 2 pseudogene 2 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ZNRF2P2 transcript	NR_027347.1:n.	N/A	Upstream 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	(T)₁₈=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₉
GRCh38.p14 chr 7	NC_000007.14:g.29686301_29686318=	NC_000007.14:g.29686314_29686318del	NC_000007.14:g.29686315_29686318del	NC_000007.14:g.29686316_29686318del	NC_000007.14:g.29686317_29686318del	NC_000007.14:g.29686318del	NC_000007.14:g.29686318dup	NC_000007.14:g.29686317_29686318dup	NC_000007.14:g.29686316_29686318dup	NC_000007.14:g.29686310_29686318dup
GRCh37.p13 chr 7	NC_000007.13:g.29725917_29725934=	NC_000007.13:g.29725930_29725934del	NC_000007.13:g.29725931_29725934del	NC_000007.13:g.29725932_29725934del	NC_000007.13:g.29725933_29725934del	NC_000007.13:g.29725934del	NC_000007.13:g.29725934dup	NC_000007.13:g.29725933_29725934dup	NC_000007.13:g.29725932_29725934dup	NC_000007.13:g.29725926_29725934dup

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#.

40 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42977257	Mar 15, 2016 (147)
2	ABI	ss43067206	Mar 15, 2016 (147)
3	HUMANGENOME_JCVI	ss95456271	Dec 05, 2013 (144)
4	HUMANGENOME_JCVI	ss98205235	Mar 15, 2016 (147)
5	BUSHMAN	ss193912609	Jul 04, 2010 (135)
6	GMI	ss288831886	May 04, 2012 (137)
7	PJP	ss295329845	May 09, 2011 (134)
8	1000GENOMES	ss1376905541	Aug 21, 2014 (142)
9	SWEGEN	ss3000849944	Nov 08, 2017 (151)
10	MCHAISSO	ss3066134504	Nov 08, 2017 (151)
11	URBANLAB	ss3648593506	Oct 12, 2018 (152)
12	EVA_DECODE	ss3719372468	Jul 13, 2019 (153)
13	EVA_DECODE	ss3719372469	Jul 13, 2019 (153)
14	EVA_DECODE	ss3719372470	Jul 13, 2019 (153)
15	EVA_DECODE	ss3719372471	Jul 13, 2019 (153)
16	EVA_DECODE	ss3719372472	Jul 13, 2019 (153)
17	PACBIO	ss3785770439	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3809525379	Jul 13, 2019 (153)
19	EVA	ss3830488403	Apr 26, 2020 (154)
20	GNOMAD	ss4160697413	Apr 26, 2021 (155)
21	GNOMAD	ss4160697414	Apr 26, 2021 (155)
22	GNOMAD	ss4160697415	Apr 26, 2021 (155)
23	GNOMAD	ss4160697416	Apr 26, 2021 (155)
24	GNOMAD	ss4160697417	Apr 26, 2021 (155)
25	GNOMAD	ss4160697418	Apr 26, 2021 (155)
26	GNOMAD	ss4160697419	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5182421267	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5182421268	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5182421269	Apr 26, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5272310301	Oct 14, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5272310302	Oct 14, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5272310303	Oct 14, 2022 (156)
33	HUGCELL_USP	ss5469548495	Oct 14, 2022 (156)
34	HUGCELL_USP	ss5469548496	Oct 14, 2022 (156)
35	HUGCELL_USP	ss5469548497	Oct 14, 2022 (156)
36	TOMMO_GENOMICS	ss5722047320	Oct 14, 2022 (156)
37	TOMMO_GENOMICS	ss5722047321	Oct 14, 2022 (156)
38	TOMMO_GENOMICS	ss5722047322	Oct 14, 2022 (156)
39	EVA	ss5822598475	Oct 14, 2022 (156)
40	EVA	ss5855824229	Oct 14, 2022 (156)
41	1000Genomes	NC_000007.13 - 29725917	Oct 12, 2018 (152)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 256848395 (NC_000007.14:29686300::T 679/126966) Row 256848396 (NC_000007.14:29686300::TT 6/126976) Row 256848397 (NC_000007.14:29686300:T: 23063/126846)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 256848395 (NC_000007.14:29686300::T 679/126966) Row 256848396 (NC_000007.14:29686300::TT 6/126976) Row 256848397 (NC_000007.14:29686300:T: 23063/126846)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 256848395 (NC_000007.14:29686300::T 679/126966) Row 256848396 (NC_000007.14:29686300::TT 6/126976) Row 256848397 (NC_000007.14:29686300:T: 23063/126846)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 256848395 (NC_000007.14:29686300::T 679/126966) Row 256848396 (NC_000007.14:29686300::TT 6/126976) Row 256848397 (NC_000007.14:29686300:T: 23063/126846)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 256848395 (NC_000007.14:29686300::T 679/126966) Row 256848396 (NC_000007.14:29686300::TT 6/126976) Row 256848397 (NC_000007.14:29686300:T: 23063/126846)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 256848395 (NC_000007.14:29686300::T 679/126966) Row 256848396 (NC_000007.14:29686300::TT 6/126976) Row 256848397 (NC_000007.14:29686300:T: 23063/126846)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 256848395 (NC_000007.14:29686300::T 679/126966) Row 256848396 (NC_000007.14:29686300::TT 6/126976) Row 256848397 (NC_000007.14:29686300:T: 23063/126846)...	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 40390574 (NC_000007.13:29725916:T: 683/16756) Row 40390575 (NC_000007.13:29725916::T 13/16756) Row 40390576 (NC_000007.13:29725916:TT: 1/16756)	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 40390574 (NC_000007.13:29725916:T: 683/16756) Row 40390575 (NC_000007.13:29725916::T 13/16756) Row 40390576 (NC_000007.13:29725916:TT: 1/16756)	-	Apr 26, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 40390574 (NC_000007.13:29725916:T: 683/16756) Row 40390575 (NC_000007.13:29725916::T 13/16756) Row 40390576 (NC_000007.13:29725916:TT: 1/16756)	-	Apr 26, 2021 (155)
52	14KJPN Submission ignored due to conflicting rows: Row 55884424 (NC_000007.14:29686300:T: 1120/28256) Row 55884425 (NC_000007.14:29686300::T 17/28256) Row 55884426 (NC_000007.14:29686300:TT: 2/28256)	-	Oct 14, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 55884424 (NC_000007.14:29686300:T: 1120/28256) Row 55884425 (NC_000007.14:29686300::T 17/28256) Row 55884426 (NC_000007.14:29686300:TT: 2/28256)	-	Oct 14, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 55884424 (NC_000007.14:29686300:T: 1120/28256) Row 55884425 (NC_000007.14:29686300::T 17/28256) Row 55884426 (NC_000007.14:29686300:TT: 2/28256)	-	Oct 14, 2022 (156)
55	ALFA	NC_000007.14 - 29686301	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)
rs199806083	May 11, 2012 (137)
rs398004210	Jul 01, 2015 (144)
rs71557434	Dec 02, 2009 (131)
rs113698722	Oct 11, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4160697419	NC_000007.14:29686300:TTTTT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4160697418	NC_000007.14:29686300:TTTT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3719372468, ss4160697417	NC_000007.14:29686300:TTT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2146896703	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3000849944, ss3830488403, ss5182421269, ss5822598475	NC_000007.13:29725916:TT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3066134504, ss4160697416, ss5272310302, ss5469548495, ss5722047322	NC_000007.14:29686300:TT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2146896703	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3719372469	NC_000007.14:29686301:TT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss42977257	NT_007819.17:29715916:TT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss193912609	NT_007819.18:29676300:TT:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss288831886	NC_000007.12:29692441:T:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss295329845	NC_000007.12:29692458:T:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
36427514, ss1376905541, ss3785770439, ss5182421267	NC_000007.13:29725916:T:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3648593506, ss3809525379, ss4160697415, ss5272310301, ss5469548496, ss5722047320, ss5855824229	NC_000007.14:29686300:T:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
2146896703	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3719372470	NC_000007.14:29686302:T:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss43067206, ss98205235	NT_007819.17:29715916:T:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss42977257	NT_007819.17:29715916:TT:T	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss95456271	NT_007819.17:29715933:T:	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5182421268	NC_000007.13:29725916::T	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4160697413, ss5272310303, ss5469548497, ss5722047321	NC_000007.14:29686300::T	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2146896703	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3719372471	NC_000007.14:29686303::T	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4160697414	NC_000007.14:29686300::TT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2146896703	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2146896703	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3719372472	NC_000007.14:29686303::TTTTTTTTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3526049527	NC_000007.14:29686300::TTT	NC_000007.14:29686300:TTTTTTTTTTTT… NC_000007.14:29686300:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

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

No publications for rs33966783

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

rs33966783