Name: rs78884990
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.

rs78884990

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:52736922-52736934 (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
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.2935 (2080/7086, ALFA)
delTT=0.3598 (1802/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF611 : 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	7086	TTTTTTTTTTTTT=0.7027	TTTTTTTTTT=0.0001, TTTTTTTTTTT=0.2935, TTTTTTTTTTTT=0.0037, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	0.56298	0.15155	0.285471	32
European	Sub	6204	TTTTTTTTTTTTT=0.6607	TTTTTTTTTT=0.0002, TTTTTTTTTTT=0.3349, TTTTTTTTTTTT=0.0042, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	0.500975	0.173277	0.325748	32
African	Sub	482	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	460	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	38	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	24	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	56	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	168	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	16	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	122	TTTTTTTTTTTTT=0.984	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.016, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	0.967213	0.0	0.032787	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	7086	(T)₁₃=0.7027	delTTT=0.0001, delTT=0.2935, delT=0.0037, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	6204	(T)₁₃=0.6607	delTTT=0.0002, delTT=0.3349, delT=0.0042, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	482	(T)₁₃=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	168	(T)₁₃=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	122	(T)₁₃=0.984	delTTT=0.000, delTT=0.016, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	56	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	38	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	16	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₃=0.6402	delTT=0.3598
1000Genomes	African	Sub	1322	(T)₁₃=0.5998	delTT=0.4002
1000Genomes	East Asian	Sub	1008	(T)₁₃=0.6558	delTT=0.3442
1000Genomes	Europe	Sub	1006	(T)₁₃=0.6471	delTT=0.3529
1000Genomes	South Asian	Sub	978	(T)₁₃=0.651	delTT=0.349
1000Genomes	American	Sub	694	(T)₁₃=0.669	delTT=0.331

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 19	NC_000019.10:g.52736931_52736934del
GRCh38.p14 chr 19	NC_000019.10:g.52736932_52736934del
GRCh38.p14 chr 19	NC_000019.10:g.52736933_52736934del
GRCh38.p14 chr 19	NC_000019.10:g.52736934del
GRCh38.p14 chr 19	NC_000019.10:g.52736934dup
GRCh38.p14 chr 19	NC_000019.10:g.52736933_52736934dup
GRCh37.p13 chr 19	NC_000019.9:g.53240184_53240187del
GRCh37.p13 chr 19	NC_000019.9:g.53240185_53240187del
GRCh37.p13 chr 19	NC_000019.9:g.53240186_53240187del
GRCh37.p13 chr 19	NC_000019.9:g.53240187del
GRCh37.p13 chr 19	NC_000019.9:g.53240187dup
GRCh37.p13 chr 19	NC_000019.9:g.53240186_53240187dup

Gene: ZNF611, zinc finger protein 611 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF611 transcript variant 2	NM_001161499.2:c.	N/A	Upstream Transcript Variant
ZNF611 transcript variant 3	NM_001161500.2:c.	N/A	Upstream Transcript Variant
ZNF611 transcript variant 4	NM_001161501.1:c.	N/A	Upstream Transcript Variant
ZNF611 transcript variant 1	NM_030972.3:c.	N/A	N/A

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)₄	delTTT	delTT	delT	dupT	dupTT
GRCh38.p14 chr 19	NC_000019.10:g.52736922_52736934=	NC_000019.10:g.52736931_52736934del	NC_000019.10:g.52736932_52736934del	NC_000019.10:g.52736933_52736934del	NC_000019.10:g.52736934del	NC_000019.10:g.52736934dup	NC_000019.10:g.52736933_52736934dup
GRCh37.p13 chr 19	NC_000019.9:g.53240175_53240187=	NC_000019.9:g.53240184_53240187del	NC_000019.9:g.53240185_53240187del	NC_000019.9:g.53240186_53240187del	NC_000019.9:g.53240187del	NC_000019.9:g.53240187dup	NC_000019.9:g.53240186_53240187dup

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, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss96282736	Mar 15, 2016 (147)
2	BCMHGSC_JDW	ss103618741	Dec 01, 2009 (131)
3	BILGI_BIOE	ss666735172	Apr 25, 2013 (138)
4	1000GENOMES	ss1378250855	Aug 21, 2014 (142)
5	DDI	ss1536896836	Apr 01, 2015 (144)
6	HAMMER_LAB	ss1809356428	Sep 08, 2015 (146)
7	SYSTEMSBIOZJU	ss2629360746	Nov 08, 2017 (151)
8	SWEGEN	ss3017650090	Nov 08, 2017 (151)
9	URBANLAB	ss3650939143	Oct 12, 2018 (152)
10	EVA_DECODE	ss3702973899	Jul 13, 2019 (153)
11	EVA_DECODE	ss3702973900	Jul 13, 2019 (153)
12	EVA_DECODE	ss3702973901	Jul 13, 2019 (153)
13	EVA_DECODE	ss3702973902	Jul 13, 2019 (153)
14	ACPOP	ss3743129458	Jul 13, 2019 (153)
15	ACPOP	ss3743129459	Jul 13, 2019 (153)
16	ACPOP	ss3743129460	Jul 13, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3821435551	Jul 13, 2019 (153)
18	EVA	ss3835515851	Apr 27, 2020 (154)
19	KOGIC	ss3981584805	Apr 27, 2020 (154)
20	KOGIC	ss3981584806	Apr 27, 2020 (154)
21	KOGIC	ss3981584807	Apr 27, 2020 (154)
22	GNOMAD	ss4332982461	Apr 27, 2021 (155)
23	GNOMAD	ss4332982462	Apr 27, 2021 (155)
24	GNOMAD	ss4332982464	Apr 27, 2021 (155)
25	GNOMAD	ss4332982465	Apr 27, 2021 (155)
26	GNOMAD	ss4332982466	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5228255100	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5228255101	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5228255102	Apr 27, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5307626917	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5307626918	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5307626919	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5307626920	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5500088271	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5500088272	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5500088273	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5500088274	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5787055856	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5787055857	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5787055858	Oct 16, 2022 (156)
41	YY_MCH	ss5817693100	Oct 16, 2022 (156)
42	EVA	ss5840694951	Oct 16, 2022 (156)
43	EVA	ss5852329221	Oct 16, 2022 (156)
44	EVA	ss5981064719	Oct 16, 2022 (156)
45	1000Genomes	NC_000019.9 - 53240175	Oct 12, 2018 (152)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542957729 (NC_000019.10:52736921::T 685/128376) Row 542957730 (NC_000019.10:52736921::TT 3/128406) Row 542957732 (NC_000019.10:52736921:T: 2808/128316)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542957729 (NC_000019.10:52736921::T 685/128376) Row 542957730 (NC_000019.10:52736921::TT 3/128406) Row 542957732 (NC_000019.10:52736921:T: 2808/128316)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542957729 (NC_000019.10:52736921::T 685/128376) Row 542957730 (NC_000019.10:52736921::TT 3/128406) Row 542957732 (NC_000019.10:52736921:T: 2808/128316)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542957729 (NC_000019.10:52736921::T 685/128376) Row 542957730 (NC_000019.10:52736921::TT 3/128406) Row 542957732 (NC_000019.10:52736921:T: 2808/128316)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542957729 (NC_000019.10:52736921::T 685/128376) Row 542957730 (NC_000019.10:52736921::TT 3/128406) Row 542957732 (NC_000019.10:52736921:T: 2808/128316)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542957729 (NC_000019.10:52736921::T 685/128376) Row 542957730 (NC_000019.10:52736921::TT 3/128406) Row 542957732 (NC_000019.10:52736921:T: 2808/128316)...	-	Apr 27, 2021 (155)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 37962806 (NC_000019.10:52736921:TT: 915/1830) Row 37962807 (NC_000019.10:52736922:T: 23/1830) Row 37962808 (NC_000019.10:52736923::T 30/1830)	-	Apr 27, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 37962806 (NC_000019.10:52736921:TT: 915/1830) Row 37962807 (NC_000019.10:52736922:T: 23/1830) Row 37962808 (NC_000019.10:52736923::T 30/1830)	-	Apr 27, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 37962806 (NC_000019.10:52736921:TT: 915/1830) Row 37962807 (NC_000019.10:52736922:T: 23/1830) Row 37962808 (NC_000019.10:52736923::T 30/1830)	-	Apr 27, 2020 (154)
55	Northern Sweden Submission ignored due to conflicting rows: Row 16414323 (NC_000019.9:53240174:TT: 278/600) Row 16414324 (NC_000019.9:53240174:T: 8/600) Row 16414325 (NC_000019.9:53240174::T 3/600)	-	Jul 13, 2019 (153)
56	Northern Sweden Submission ignored due to conflicting rows: Row 16414323 (NC_000019.9:53240174:TT: 278/600) Row 16414324 (NC_000019.9:53240174:T: 8/600) Row 16414325 (NC_000019.9:53240174::T 3/600)	-	Jul 13, 2019 (153)
57	Northern Sweden Submission ignored due to conflicting rows: Row 16414323 (NC_000019.9:53240174:TT: 278/600) Row 16414324 (NC_000019.9:53240174:T: 8/600) Row 16414325 (NC_000019.9:53240174::T 3/600)	-	Jul 13, 2019 (153)
58	8.3KJPN Submission ignored due to conflicting rows: Row 86224407 (NC_000019.9:53240174:TT: 8716/16734) Row 86224408 (NC_000019.9:53240174::T 14/16734) Row 86224409 (NC_000019.9:53240174:T: 42/16734)	-	Apr 27, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 86224407 (NC_000019.9:53240174:TT: 8716/16734) Row 86224408 (NC_000019.9:53240174::T 14/16734) Row 86224409 (NC_000019.9:53240174:T: 42/16734)	-	Apr 27, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 86224407 (NC_000019.9:53240174:TT: 8716/16734) Row 86224408 (NC_000019.9:53240174::T 14/16734) Row 86224409 (NC_000019.9:53240174:T: 42/16734)	-	Apr 27, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 120892960 (NC_000019.10:52736921:TT: 14742/28232) Row 120892961 (NC_000019.10:52736921:T: 76/28232) Row 120892962 (NC_000019.10:52736921::T 23/28232)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 120892960 (NC_000019.10:52736921:TT: 14742/28232) Row 120892961 (NC_000019.10:52736921:T: 76/28232) Row 120892962 (NC_000019.10:52736921::T 23/28232)	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 120892960 (NC_000019.10:52736921:TT: 14742/28232) Row 120892961 (NC_000019.10:52736921:T: 76/28232) Row 120892962 (NC_000019.10:52736921::T 23/28232)	-	Oct 16, 2022 (156)
64	ALFA	NC_000019.10 - 52736922	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
ss4332982466	NC_000019.10:52736921:TTTT:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3702973899, ss4332982465, ss5307626919, ss5500088274	NC_000019.10:52736921:TTT:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
3176125852	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTT	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
76990217, ss666735172, ss1378250855, ss1536896836, ss1809356428, ss2629360746, ss3017650090, ss3743129458, ss3835515851, ss5228255100, ss5840694951, ss5981064719	NC_000019.9:53240174:TT:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3650939143, ss3821435551, ss3981584805, ss4332982464, ss5307626917, ss5500088271, ss5787055856, ss5817693100, ss5852329221	NC_000019.10:52736921:TT:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
3176125852	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3702973900	NC_000019.10:52736922:TT:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss96282736	NT_011109.16:25508392:TT:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss103618741	NT_011109.16:25508403:TT:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3743129459, ss5228255102	NC_000019.9:53240174:T:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5307626918, ss5500088272, ss5787055857	NC_000019.10:52736921:T:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3176125852	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3981584806	NC_000019.10:52736922:T:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3702973901	NC_000019.10:52736923:T:	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3743129460, ss5228255101	NC_000019.9:53240174::T	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4332982461, ss5307626920, ss5500088273, ss5787055858	NC_000019.10:52736921::T	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3176125852	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3981584807	NC_000019.10:52736923::T	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3702973902	NC_000019.10:52736924::T	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4332982462	NC_000019.10:52736921::TT	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3176125852	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:52736921:TTTTTTTTTTTT… NC_000019.10:52736921:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(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 rs78884990

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

rs78884990