Name: rs33911235
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.

rs33911235

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:181071654-181071670 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.2871 (1964/6842, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00290 : 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	6842	TTTTTTTTTTTTTTTTT=0.6894	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTT=0.0219, TTTTTTTTTTTTTTTTTT=0.2871, TTTTTTTTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.604167	0.183517	0.212316	32
European	Sub	5664	TTTTTTTTTTTTTTTTT=0.6254	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTT=0.0265, TTTTTTTTTTTTTTTTTT=0.3462, TTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.517757	0.223551	0.258692	32
African	Sub	934	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	896	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	24	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	94	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	30	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	94	TTTTTTTTTTTTTTTTT=0.97	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	0.957447	0.021277	0.021277	11

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	6842	(T)₁₇=0.6894	delTTT=0.0000, delTT=0.0003, delT=0.0219, dupT=0.2871, dupTT=0.0013, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	5664	(T)₁₇=0.6254	delTTT=0.0000, delTT=0.0004, delT=0.0265, dupT=0.3462, dupTT=0.0016, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	934	(T)₁₇=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	94	(T)₁₇=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Other	Sub	94	(T)₁₇=0.97	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.03, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(T)₁₇=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	24	(T)₁₇=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	2	(T)₁₇=1.0	delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0

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 4	NC_000004.12:g.181071667_181071670del
GRCh38.p14 chr 4	NC_000004.12:g.181071668_181071670del
GRCh38.p14 chr 4	NC_000004.12:g.181071669_181071670del
GRCh38.p14 chr 4	NC_000004.12:g.181071670del
GRCh38.p14 chr 4	NC_000004.12:g.181071670dup
GRCh38.p14 chr 4	NC_000004.12:g.181071669_181071670dup
GRCh38.p14 chr 4	NC_000004.12:g.181071668_181071670dup
GRCh38.p14 chr 4	NC_000004.12:g.181071667_181071670dup
GRCh38.p14 chr 4	NC_000004.12:g.181071661_181071670dup
GRCh37.p13 chr 4	NC_000004.11:g.181992820_181992823del
GRCh37.p13 chr 4	NC_000004.11:g.181992821_181992823del
GRCh37.p13 chr 4	NC_000004.11:g.181992822_181992823del
GRCh37.p13 chr 4	NC_000004.11:g.181992823del
GRCh37.p13 chr 4	NC_000004.11:g.181992823dup
GRCh37.p13 chr 4	NC_000004.11:g.181992822_181992823dup
GRCh37.p13 chr 4	NC_000004.11:g.181992821_181992823dup
GRCh37.p13 chr 4	NC_000004.11:g.181992820_181992823dup
GRCh37.p13 chr 4	NC_000004.11:g.181992814_181992823dup

Gene: LINC00290, long intergenic non-protein coding RNA 290 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00290 transcript	NR_033918.1:n.	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)₁₇=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₁₀
GRCh38.p14 chr 4	NC_000004.12:g.181071654_181071670=	NC_000004.12:g.181071667_181071670del	NC_000004.12:g.181071668_181071670del	NC_000004.12:g.181071669_181071670del	NC_000004.12:g.181071670del	NC_000004.12:g.181071670dup	NC_000004.12:g.181071669_181071670dup	NC_000004.12:g.181071668_181071670dup	NC_000004.12:g.181071667_181071670dup	NC_000004.12:g.181071661_181071670dup
GRCh37.p13 chr 4	NC_000004.11:g.181992807_181992823=	NC_000004.11:g.181992820_181992823del	NC_000004.11:g.181992821_181992823del	NC_000004.11:g.181992822_181992823del	NC_000004.11:g.181992823del	NC_000004.11:g.181992823dup	NC_000004.11:g.181992822_181992823dup	NC_000004.11:g.181992821_181992823dup	NC_000004.11:g.181992820_181992823dup	NC_000004.11:g.181992814_181992823dup

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#.

39 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79739166	Sep 08, 2015 (146)
2	PJP	ss295204703	May 09, 2011 (137)
3	BILGI_BIOE	ss666292351	Apr 25, 2013 (138)
4	EVA_UK10K_ALSPAC	ss1704499075	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1704499076	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1704502071	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1704502072	Apr 01, 2015 (144)
8	SWEGEN	ss2996150246	Nov 08, 2017 (151)
9	MCHAISSO	ss3064138351	Nov 08, 2017 (151)
10	MCHAISSO	ss3065007326	Nov 08, 2017 (151)
11	MCHAISSO	ss3065993560	Nov 08, 2017 (151)
12	EVA_DECODE	ss3713779628	Jul 13, 2019 (153)
13	EVA_DECODE	ss3713779629	Jul 13, 2019 (153)
14	EVA_DECODE	ss3713779630	Jul 13, 2019 (153)
15	EVA_DECODE	ss3713779631	Jul 13, 2019 (153)
16	EVA	ss3829002707	Apr 26, 2020 (154)
17	GNOMAD	ss4096726272	Apr 26, 2021 (155)
18	GNOMAD	ss4096726273	Apr 26, 2021 (155)
19	GNOMAD	ss4096726274	Apr 26, 2021 (155)
20	GNOMAD	ss4096726275	Apr 26, 2021 (155)
21	GNOMAD	ss4096726277	Apr 26, 2021 (155)
22	GNOMAD	ss4096726278	Apr 26, 2021 (155)
23	GNOMAD	ss4096726279	Apr 26, 2021 (155)
24	GNOMAD	ss4096726280	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5169639982	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5169639983	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5169639984	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5169639985	Apr 26, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5262302454	Oct 13, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5262302455	Oct 13, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5262302456	Oct 13, 2022 (156)
32	HUGCELL_USP	ss5460723439	Oct 13, 2022 (156)
33	HUGCELL_USP	ss5460723440	Oct 13, 2022 (156)
34	TOMMO_GENOMICS	ss5705080324	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5705080325	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5705080326	Oct 13, 2022 (156)
37	EVA	ss5845223904	Oct 13, 2022 (156)
38	EVA	ss5845223905	Oct 13, 2022 (156)
39	EVA	ss5854605024	Oct 13, 2022 (156)
40	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 13801394 (NC_000004.11:181992806::T 1626/3854) Row 13801395 (NC_000004.11:181992806::TT 468/3854)	-	Oct 12, 2018 (152)
41	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 13801394 (NC_000004.11:181992806::T 1626/3854) Row 13801395 (NC_000004.11:181992806::TT 468/3854)	-	Oct 12, 2018 (152)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 175540314 (NC_000004.12:181071653::T 60799/126364) Row 175540315 (NC_000004.12:181071653::TT 319/126352) Row 175540316 (NC_000004.12:181071653::TTT 9/126382)...	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 27609289 (NC_000004.11:181992806:T: 1167/16702) Row 27609290 (NC_000004.11:181992806::T 10451/16702) Row 27609291 (NC_000004.11:181992806::TT 29/16702)...	-	Apr 26, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 27609289 (NC_000004.11:181992806:T: 1167/16702) Row 27609290 (NC_000004.11:181992806::T 10451/16702) Row 27609291 (NC_000004.11:181992806::TT 29/16702)...	-	Apr 26, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 27609289 (NC_000004.11:181992806:T: 1167/16702) Row 27609290 (NC_000004.11:181992806::T 10451/16702) Row 27609291 (NC_000004.11:181992806::TT 29/16702)...	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 27609289 (NC_000004.11:181992806:T: 1167/16702) Row 27609290 (NC_000004.11:181992806::T 10451/16702) Row 27609291 (NC_000004.11:181992806::TT 29/16702)...	-	Apr 26, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 38917428 (NC_000004.12:181071653:T: 1931/28258) Row 38917429 (NC_000004.12:181071653::T 18013/28258) Row 38917430 (NC_000004.12:181071653::TT 34/28258)	-	Oct 13, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 38917428 (NC_000004.12:181071653:T: 1931/28258) Row 38917429 (NC_000004.12:181071653::T 18013/28258) Row 38917430 (NC_000004.12:181071653::TT 34/28258)	-	Oct 13, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 38917428 (NC_000004.12:181071653:T: 1931/28258) Row 38917429 (NC_000004.12:181071653::T 18013/28258) Row 38917430 (NC_000004.12:181071653::TT 34/28258)	-	Oct 13, 2022 (156)
57	UK 10K study - Twins Submission ignored due to conflicting rows: Row 13801394 (NC_000004.11:181992806::T 1511/3708) Row 13801395 (NC_000004.11:181992806::TT 453/3708)	-	Oct 12, 2018 (152)
58	UK 10K study - Twins Submission ignored due to conflicting rows: Row 13801394 (NC_000004.11:181992806::T 1511/3708) Row 13801395 (NC_000004.11:181992806::TT 453/3708)	-	Oct 12, 2018 (152)
59	ALFA	NC_000004.12 - 181071654	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)
rs57043127	May 11, 2012 (137)
rs147428938	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4096726280	NC_000004.12:181071653:TTTT:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5169639985	NC_000004.11:181992806:TTT:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4096726279	NC_000004.12:181071653:TTT:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12199885921	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4096726278	NC_000004.12:181071653:TT:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12199885921	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss79739166	NC_000004.9:182367971:T:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss295204703	NC_000004.10:182229800:T:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss2996150246, ss5169639982	NC_000004.11:181992806:T:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3713779628, ss4096726277, ss5262302454, ss5460723439, ss5705080324	NC_000004.12:181071653:T:	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12199885921	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss666292351, ss1704499075, ss1704502071, ss3829002707, ss5169639983, ss5845223904	NC_000004.11:181992806::T	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3064138351, ss3065007326, ss3065993560, ss4096726272, ss5262302455, ss5460723440, ss5705080325, ss5854605024	NC_000004.12:181071653::T	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
12199885921	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3713779629	NC_000004.12:181071654::T	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1704499076, ss1704502072, ss5169639984, ss5845223905	NC_000004.11:181992806::TT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4096726273, ss5262302456, ss5705080326	NC_000004.12:181071653::TT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12199885921	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3713779630	NC_000004.12:181071654::TT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4096726274	NC_000004.12:181071653::TTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12199885921	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4096726275	NC_000004.12:181071653::TTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12199885921	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3713779631	NC_000004.12:181071654::TTTTTTTTTT	NC_000004.12:181071653:TTTTTTTTTTT… NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs33911235

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

rs33911235