Name: rs796119778
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.

rs796119778

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr21:34767335-34767350 (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
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.2286 (1607/7030, ALFA)
dupT=0.3844 (1925/5008, 1000G)
dupT=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01426 : 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	7030	TTTTTTTTTTTTTTTT=0.7622	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTTT=0.2286, TTTTTTTTTTTTTTTTTT=0.0088, TTTTTTTTTTTTTTTTTTT=0.0000	0.660683	0.117834	0.221482	32
European	Sub	5958	TTTTTTTTTTTTTTTT=0.7197	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTT=0.2694, TTTTTTTTTTTTTTTTTT=0.0104, TTTTTTTTTTTTTTTTTTT=0.0000	0.59904	0.139479	0.26148	32
African	Sub	726	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	694	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	32	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	28	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	24	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	162	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	26	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	102	TTTTTTTTTTTTTTTT=0.980	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.020, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	0.960784	0.0	0.039216	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
Allele Frequency Aggregator	Total	Global	7030	(T)₁₆=0.7622	del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0004, dupT=0.2286, dupTT=0.0088, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	5958	(T)₁₆=0.7197	del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0005, dupT=0.2694, dupTT=0.0104, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	726	(T)₁₆=1.000	del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	162	(T)₁₆=1.000	del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	102	(T)₁₆=0.980	del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.020, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	32	(T)₁₆=1.00	del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(T)₁₆=1.00	del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	24	(T)₁₆=1.00	del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.3844
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.3359
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.3581
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.4443
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.424
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.372
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.38

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.34767346_34767350del
GRCh38.p14 chr 21	NC_000021.9:g.34767347_34767350del
GRCh38.p14 chr 21	NC_000021.9:g.34767348_34767350del
GRCh38.p14 chr 21	NC_000021.9:g.34767349_34767350del
GRCh38.p14 chr 21	NC_000021.9:g.34767350del
GRCh38.p14 chr 21	NC_000021.9:g.34767350dup
GRCh38.p14 chr 21	NC_000021.9:g.34767349_34767350dup
GRCh38.p14 chr 21	NC_000021.9:g.34767348_34767350dup
GRCh37.p13 chr 21	NC_000021.8:g.36139643_36139647del
GRCh37.p13 chr 21	NC_000021.8:g.36139644_36139647del
GRCh37.p13 chr 21	NC_000021.8:g.36139645_36139647del
GRCh37.p13 chr 21	NC_000021.8:g.36139646_36139647del
GRCh37.p13 chr 21	NC_000021.8:g.36139647del
GRCh37.p13 chr 21	NC_000021.8:g.36139647dup
GRCh37.p13 chr 21	NC_000021.8:g.36139646_36139647dup
GRCh37.p13 chr 21	NC_000021.8:g.36139645_36139647dup

Gene: LINC01426, long intergenic non-protein coding RNA 1426 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01426 transcript variant 1	NR_038885.1:n.	N/A	Intron Variant
LINC01426 transcript variant 2	NR_038886.1:n.	N/A	Genic Downstream 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)₁₆=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 21	NC_000021.9:g.34767335_34767350=	NC_000021.9:g.34767346_34767350del	NC_000021.9:g.34767347_34767350del	NC_000021.9:g.34767348_34767350del	NC_000021.9:g.34767349_34767350del	NC_000021.9:g.34767350del	NC_000021.9:g.34767350dup	NC_000021.9:g.34767349_34767350dup	NC_000021.9:g.34767348_34767350dup
GRCh37.p13 chr 21	NC_000021.8:g.36139632_36139647=	NC_000021.8:g.36139643_36139647del	NC_000021.8:g.36139644_36139647del	NC_000021.8:g.36139645_36139647del	NC_000021.8:g.36139646_36139647del	NC_000021.8:g.36139647del	NC_000021.8:g.36139647dup	NC_000021.8:g.36139646_36139647dup	NC_000021.8:g.36139645_36139647dup

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#.

42 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81904757	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95750698	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss96177772	Oct 12, 2018 (152)
4	GMI	ss289433651	Oct 12, 2018 (152)
5	PJP	ss295066956	Oct 12, 2018 (152)
6	PJP	ss295066957	Oct 12, 2018 (152)
7	1000GENOMES	ss1378779436	Oct 12, 2018 (152)
8	EVA_GENOME_DK	ss1575778320	Oct 12, 2018 (152)
9	HAMMER_LAB	ss1809674991	Sep 08, 2015 (146)
10	SWEGEN	ss3018855246	Nov 08, 2017 (151)
11	MCHAISSO	ss3065840456	Nov 08, 2017 (151)
12	EVA_DECODE	ss3707685427	Jul 13, 2019 (153)
13	EVA_DECODE	ss3707685428	Jul 13, 2019 (153)
14	EVA_DECODE	ss3707685429	Jul 13, 2019 (153)
15	KHV_HUMAN_GENOMES	ss3822247109	Jul 13, 2019 (153)
16	EVA	ss3835861765	Apr 27, 2020 (154)
17	GNOMAD	ss4359960557	Apr 27, 2021 (155)
18	GNOMAD	ss4359960558	Apr 27, 2021 (155)
19	GNOMAD	ss4359960559	Apr 27, 2021 (155)
20	GNOMAD	ss4359960560	Apr 27, 2021 (155)
21	GNOMAD	ss4359960561	Apr 27, 2021 (155)
22	GNOMAD	ss4359960562	Apr 27, 2021 (155)
23	GNOMAD	ss4359960563	Apr 27, 2021 (155)
24	GNOMAD	ss4359960564	Apr 27, 2021 (155)
25	TOMMO_GENOMICS	ss5231435364	Apr 27, 2021 (155)
26	TOMMO_GENOMICS	ss5231435365	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5231435366	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5231435367	Apr 27, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5310142023	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5310142024	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5310142025	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5310142026	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5502195587	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5502195588	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5502195589	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5791919068	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5791919069	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5791919070	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5791919071	Oct 16, 2022 (156)
40	EVA	ss5839009357	Oct 16, 2022 (156)
41	EVA	ss5839009358	Oct 16, 2022 (156)
42	EVA	ss5853294810	Oct 16, 2022 (156)
43	1000Genomes	NC_000021.8 - 36139632	Oct 12, 2018 (152)
44	The Danish reference pan genome	NC_000021.8 - 36139632	Apr 27, 2020 (154)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 562591230 (NC_000021.9:34767334::T 64683/130516) Row 562591231 (NC_000021.9:34767334::TT 2907/130540) Row 562591232 (NC_000021.9:34767334::TTT 25/130574)...	-	Apr 27, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 89404671 (NC_000021.8:36139631::T 6419/16758) Row 89404672 (NC_000021.8:36139631:T: 23/16758) Row 89404673 (NC_000021.8:36139631::TT 484/16758)...	-	Apr 27, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 89404671 (NC_000021.8:36139631::T 6419/16758) Row 89404672 (NC_000021.8:36139631:T: 23/16758) Row 89404673 (NC_000021.8:36139631::TT 484/16758)...	-	Apr 27, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 89404671 (NC_000021.8:36139631::T 6419/16758) Row 89404672 (NC_000021.8:36139631:T: 23/16758) Row 89404673 (NC_000021.8:36139631::TT 484/16758)...	-	Apr 27, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 89404671 (NC_000021.8:36139631::T 6419/16758) Row 89404672 (NC_000021.8:36139631:T: 23/16758) Row 89404673 (NC_000021.8:36139631::TT 484/16758)...	-	Apr 27, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 125756172 (NC_000021.9:34767334::T 10760/28254) Row 125756173 (NC_000021.9:34767334::TT 807/28254) Row 125756174 (NC_000021.9:34767334:T: 40/28254)...	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 125756172 (NC_000021.9:34767334::T 10760/28254) Row 125756173 (NC_000021.9:34767334::TT 807/28254) Row 125756174 (NC_000021.9:34767334:T: 40/28254)...	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 125756172 (NC_000021.9:34767334::T 10760/28254) Row 125756173 (NC_000021.9:34767334::TT 807/28254) Row 125756174 (NC_000021.9:34767334:T: 40/28254)...	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 125756172 (NC_000021.9:34767334::T 10760/28254) Row 125756173 (NC_000021.9:34767334::TT 807/28254) Row 125756174 (NC_000021.9:34767334:T: 40/28254)...	-	Oct 16, 2022 (156)
61	ALFA	NC_000021.9 - 34767335	Apr 27, 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
ss4359960564, ss5310142026	NC_000021.9:34767334:TTTTT:	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
12713988587	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4359960563	NC_000021.9:34767334:TTTT:	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12713988587	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5231435367	NC_000021.8:36139631:TTT:	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4359960562, ss5791919071	NC_000021.9:34767334:TTT:	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4359960561	NC_000021.9:34767334:TT:	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12713988587	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3018855246, ss5231435365	NC_000021.8:36139631:T:	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3065840456, ss3707685427, ss4359960560, ss5310142025, ss5502195589, ss5791919070	NC_000021.9:34767334:T:	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12713988587	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss295066956	NC_000021.7:35061502::T	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss289433651, ss295066957	NC_000021.7:35061517::T	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
79717630, 780966, ss1378779436, ss1575778320, ss1809674991, ss3835861765, ss5231435364, ss5839009357	NC_000021.8:36139631::T	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3822247109, ss4359960557, ss5310142023, ss5502195587, ss5791919068, ss5853294810	NC_000021.9:34767334::T	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12713988587	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3707685428	NC_000021.9:34767335::T	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss96177772	NT_011512.11:21801502::T	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss81904757, ss95750698	NT_011512.11:21801518::T	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5231435366, ss5839009358	NC_000021.8:36139631::TT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4359960558, ss5310142024, ss5502195588, ss5791919069	NC_000021.9:34767334::TT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
12713988587	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3707685429	NC_000021.9:34767335::TT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4359960559	NC_000021.9:34767334::TTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12713988587	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000021.9:34767334:TTTTTTTTTTTTT… NC_000021.9:34767334:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(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 rs796119778

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

rs796119778