Name: rs35860148
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.

rs35860148

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:119599978-119599991 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1066 (1028/9648, ALFA)
delTT=0.0568 (219/3854, ALSPAC)
delTT=0.0491 (182/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00622 : 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	9648	TTTTTTTTTTTTTT=0.8806	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0088, TTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTT=0.1066, TTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTTTT=0.0009	0.817776	0.029981	0.152243	32
European	Sub	8630	TTTTTTTTTTTTTT=0.8666	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0098, TTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTT=0.1190, TTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTT=0.0010	0.795899	0.033619	0.170482	32
African	Sub	562	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	554	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	16	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	12	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	50	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	184	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	22	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	184	TTTTTTTTTTTTTT=0.995	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	0.98913	0.0	0.01087	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	9648	(T)₁₄=0.8806	delTTT=0.0000, delTT=0.0088, delT=0.0013, dupT=0.1066, dupTT=0.0007, dupTTT=0.0009, dup(T)₄=0.0010
Allele Frequency Aggregator	European	Sub	8630	(T)₁₄=0.8666	delTTT=0.0000, delTT=0.0098, delT=0.0015, dupT=0.1190, dupTT=0.0008, dupTTT=0.0010, dup(T)₄=0.0012
Allele Frequency Aggregator	African	Sub	562	(T)₁₄=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	184	(T)₁₄=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	Other	Sub	184	(T)₁₄=0.995	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.005, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(T)₁₄=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	South Asian	Sub	22	(T)₁₄=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	16	(T)₁₄=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
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₄=0.9432	delTT=0.0568
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₄=0.9509	delTT=0.0491

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 1	NC_000001.11:g.119599989_119599991del
GRCh38.p14 chr 1	NC_000001.11:g.119599990_119599991del
GRCh38.p14 chr 1	NC_000001.11:g.119599991del
GRCh38.p14 chr 1	NC_000001.11:g.119599991dup
GRCh38.p14 chr 1	NC_000001.11:g.119599990_119599991dup
GRCh38.p14 chr 1	NC_000001.11:g.119599989_119599991dup
GRCh38.p14 chr 1	NC_000001.11:g.119599988_119599991dup
GRCh38.p14 chr 1	NC_000001.11:g.119599984_119599991dup
GRCh37.p13 chr 1	NC_000001.10:g.120142612_120142614del
GRCh37.p13 chr 1	NC_000001.10:g.120142613_120142614del
GRCh37.p13 chr 1	NC_000001.10:g.120142614del
GRCh37.p13 chr 1	NC_000001.10:g.120142614dup
GRCh37.p13 chr 1	NC_000001.10:g.120142613_120142614dup
GRCh37.p13 chr 1	NC_000001.10:g.120142612_120142614dup
GRCh37.p13 chr 1	NC_000001.10:g.120142611_120142614dup
GRCh37.p13 chr 1	NC_000001.10:g.120142607_120142614dup

Gene: LINC00622, long intergenic non-protein coding RNA 622 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00622 transcript	NR_036540.1: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)₁₄=	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₈
GRCh38.p14 chr 1	NC_000001.11:g.119599978_119599991=	NC_000001.11:g.119599989_119599991del	NC_000001.11:g.119599990_119599991del	NC_000001.11:g.119599991del	NC_000001.11:g.119599991dup	NC_000001.11:g.119599990_119599991dup	NC_000001.11:g.119599989_119599991dup	NC_000001.11:g.119599988_119599991dup	NC_000001.11:g.119599984_119599991dup
GRCh37.p13 chr 1	NC_000001.10:g.120142601_120142614=	NC_000001.10:g.120142612_120142614del	NC_000001.10:g.120142613_120142614del	NC_000001.10:g.120142614del	NC_000001.10:g.120142614dup	NC_000001.10:g.120142613_120142614dup	NC_000001.10:g.120142612_120142614dup	NC_000001.10:g.120142611_120142614dup	NC_000001.10:g.120142607_120142614dup

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#.

49 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41055790	Mar 15, 2006 (126)
2	HGSV	ss80835763	Dec 03, 2013 (138)
3	HGSV	ss83071316	Dec 05, 2013 (138)
4	BUSHMAN	ss193124601	Jul 04, 2010 (132)
5	GMI	ss288032780	Oct 11, 2018 (152)
6	PJP	ss294600992	Oct 11, 2018 (152)
7	SSMP	ss663114375	Apr 01, 2015 (144)
8	DDI	ss1536245953	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1701187162	Jan 10, 2018 (151)
10	EVA_UK10K_ALSPAC	ss1701187163	Jan 10, 2018 (151)
11	HAMMER_LAB	ss1795012825	Sep 08, 2015 (146)
12	SWEGEN	ss2987530255	Jan 10, 2018 (151)
13	BEROUKHIMLAB	ss3644068077	Oct 11, 2018 (152)
14	EVA_DECODE	ss3687642461	Jul 12, 2019 (153)
15	EVA_DECODE	ss3687642462	Jul 12, 2019 (153)
16	EVA_DECODE	ss3687642464	Jul 12, 2019 (153)
17	ACPOP	ss3727437353	Jul 12, 2019 (153)
18	ACPOP	ss3727437354	Jul 12, 2019 (153)
19	PACBIO	ss3783535430	Jul 12, 2019 (153)
20	PACBIO	ss3789174817	Jul 12, 2019 (153)
21	PACBIO	ss3794047781	Jul 12, 2019 (153)
22	EVA	ss3826398920	Apr 25, 2020 (154)
23	EVA	ss3836590148	Apr 25, 2020 (154)
24	EVA	ss3841998801	Apr 25, 2020 (154)
25	KOGIC	ss3945359356	Apr 25, 2020 (154)
26	KOGIC	ss3945359357	Apr 25, 2020 (154)
27	KOGIC	ss3945359358	Apr 25, 2020 (154)
28	GNOMAD	ss4001442677	Apr 25, 2021 (155)
29	GNOMAD	ss4001442678	Apr 25, 2021 (155)
30	GNOMAD	ss4001442679	Apr 25, 2021 (155)
31	GNOMAD	ss4001442680	Apr 25, 2021 (155)
32	GNOMAD	ss4001442681	Apr 25, 2021 (155)
33	GNOMAD	ss4001442682	Apr 25, 2021 (155)
34	GNOMAD	ss4001442683	Apr 25, 2021 (155)
35	GNOMAD	ss4001442684	Apr 25, 2021 (155)
36	TOMMO_GENOMICS	ss5145936929	Apr 25, 2021 (155)
37	TOMMO_GENOMICS	ss5145936930	Apr 25, 2021 (155)
38	TOMMO_GENOMICS	ss5145936931	Apr 25, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5243806376	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5243806377	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5444709007	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5444709008	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5444709009	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5444709010	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5671279463	Oct 12, 2022 (156)
46	TOMMO_GENOMICS	ss5671279464	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5671279465	Oct 12, 2022 (156)
48	EVA	ss5832560608	Oct 12, 2022 (156)
49	EVA	ss5938283591	Oct 12, 2022 (156)
50	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 120142601	Oct 11, 2018 (152)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 24368315 (NC_000001.11:119599977::T 30026/135480) Row 24368316 (NC_000001.11:119599977::TT 76/135600) Row 24368317 (NC_000001.11:119599977::TTT 3/135624)...	-	Apr 25, 2021 (155)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 1737357 (NC_000001.11:119599978::T 1000/1832) Row 1737358 (NC_000001.11:119599977:T: 48/1832) Row 1737359 (NC_000001.11:119599978::TT 49/1832)	-	Apr 25, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 1737357 (NC_000001.11:119599978::T 1000/1832) Row 1737358 (NC_000001.11:119599977:T: 48/1832) Row 1737359 (NC_000001.11:119599978::TT 49/1832)	-	Apr 25, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 1737357 (NC_000001.11:119599978::T 1000/1832) Row 1737358 (NC_000001.11:119599977:T: 48/1832) Row 1737359 (NC_000001.11:119599978::TT 49/1832)	-	Apr 25, 2020 (154)
62	Northern Sweden Submission ignored due to conflicting rows: Row 722218 (NC_000001.10:120142600::T 101/598) Row 722219 (NC_000001.10:120142600:TT: 31/598)	-	Jul 12, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 722218 (NC_000001.10:120142600::T 101/598) Row 722219 (NC_000001.10:120142600:TT: 31/598)	-	Jul 12, 2019 (153)
64	8.3KJPN Submission ignored due to conflicting rows: Row 3906236 (NC_000001.10:120142600::T 10316/16758) Row 3906237 (NC_000001.10:120142600:T: 291/16758) Row 3906238 (NC_000001.10:120142600::TT 19/16758)	-	Apr 25, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 3906236 (NC_000001.10:120142600::T 10316/16758) Row 3906237 (NC_000001.10:120142600:T: 291/16758) Row 3906238 (NC_000001.10:120142600::TT 19/16758)	-	Apr 25, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 3906236 (NC_000001.10:120142600::T 10316/16758) Row 3906237 (NC_000001.10:120142600:T: 291/16758) Row 3906238 (NC_000001.10:120142600::TT 19/16758)	-	Apr 25, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 5116567 (NC_000001.11:119599977::T 17305/28254) Row 5116568 (NC_000001.11:119599977:T: 511/28254) Row 5116569 (NC_000001.11:119599977::TT 27/28254)	-	Oct 12, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 5116567 (NC_000001.11:119599977::T 17305/28254) Row 5116568 (NC_000001.11:119599977:T: 511/28254) Row 5116569 (NC_000001.11:119599977::TT 27/28254)	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 5116567 (NC_000001.11:119599977::T 17305/28254) Row 5116568 (NC_000001.11:119599977:T: 511/28254) Row 5116569 (NC_000001.11:119599977::TT 27/28254)	-	Oct 12, 2022 (156)
70	UK 10K study - Twins	NC_000001.10 - 120142601	Oct 11, 2018 (152)
71	ALFA	NC_000001.11 - 119599978	Apr 25, 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
ss4001442684	NC_000001.11:119599977:TTT:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
4975510449	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
1910339, 1910339, ss1701187162, ss1701187163, ss2987530255, ss3727437354, ss5832560608, ss5938283591	NC_000001.10:120142600:TT:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3687642461, ss4001442683, ss5243806377, ss5444709009	NC_000001.11:119599977:TT:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4975510449	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5145936930	NC_000001.10:120142600:T:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3945359357, ss4001442682, ss5444709007, ss5671279464	NC_000001.11:119599977:T:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4975510449	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3687642462	NC_000001.11:119599978:T:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss41055790	NT_032977.9:90114518:T:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss193124601	NT_032977.10:119013989:T:	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss294600992	NC_000001.9:119944131::T	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss288032780	NC_000001.9:119944137::T	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss663114375, ss1536245953, ss1795012825, ss3644068077, ss3727437353, ss3783535430, ss3789174817, ss3794047781, ss3826398920, ss3836590148, ss5145936929	NC_000001.10:120142600::T	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3841998801, ss4001442677, ss5243806376, ss5444709008, ss5671279463	NC_000001.11:119599977::T	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4975510449	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3945359356	NC_000001.11:119599978::T	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3687642464	NC_000001.11:119599979::T	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss80835763, ss83071316	NT_032977.9:90114532::T	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5145936931	NC_000001.10:120142600::TT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4001442678, ss5444709010, ss5671279465	NC_000001.11:119599977::TT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4975510449	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3945359358	NC_000001.11:119599978::TT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4001442679	NC_000001.11:119599977::TTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4975510449	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4001442680	NC_000001.11:119599977::TTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4975510449	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4001442681	NC_000001.11:119599977::TTTTTTTT	NC_000001.11:119599977:TTTTTTTTTTT… NC_000001.11:119599977:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(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 rs35860148

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

rs35860148