Name: rs35074350
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.

rs35074350

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:157753923-157753933 (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: delTT / delT / dupT / dupTT / dup(…
delTT / delT / dupT / dupTT / dup(T)₆ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.1954 (1565/8010, ALFA)
delTT=0.0030 (7/2367, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LSM11 : 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	8010	TTTTTTTTTTT=0.7589	TTTTTTTTT=0.0000, TTTTTTTTTT=0.1954, TTTTTTTTTTTT=0.0457, TTTTTTTTTTTTT=0.0000	0.687296	0.076063	0.236641	32
European	Sub	6696	TTTTTTTTTTT=0.7124	TTTTTTTTT=0.0000, TTTTTTTTTT=0.2331, TTTTTTTTTTTT=0.0545, TTTTTTTTTTTTT=0.0000	0.619854	0.092297	0.287849	32
African	Sub	816	TTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	794	TTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	24	TTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	18	TTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	52	TTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	226	TTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	32	TTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	164	TTTTTTTTTTT=0.970	TTTTTTTTT=0.000, TTTTTTTTTT=0.024, TTTTTTTTTTTT=0.006, TTTTTTTTTTTTT=0.000	0.975309	0.012346	0.012346	19

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	8010	(T)₁₁=0.7589	delTT=0.0000, delT=0.1954, dupT=0.0457, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	6696	(T)₁₁=0.7124	delTT=0.0000, delT=0.2331, dupT=0.0545, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	816	(T)₁₁=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	226	(T)₁₁=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	164	(T)₁₁=0.970	delTT=0.000, delT=0.024, dupT=0.006, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	52	(T)₁₁=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(T)₁₁=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	24	(T)₁₁=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	2367	(T)₁₁=0.9970	delTT=0.0030
1000Genomes	African	Sub	630	(T)₁₁=0.997	delTT=0.003
1000Genomes	Europe	Sub	497	(T)₁₁=1.000	delTT=0.000
1000Genomes	South Asian	Sub	490	(T)₁₁=0.998	delTT=0.002
1000Genomes	East Asian	Sub	384	(T)₁₁=0.995	delTT=0.005
1000Genomes	American	Sub	366	(T)₁₁=0.995	delTT=0.005

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 5	NC_000005.10:g.157753932_157753933del
GRCh38.p14 chr 5	NC_000005.10:g.157753933del
GRCh38.p14 chr 5	NC_000005.10:g.157753933dup
GRCh38.p14 chr 5	NC_000005.10:g.157753932_157753933dup
GRCh38.p14 chr 5	NC_000005.10:g.157753928_157753933dup
GRCh38.p14 chr 5	NC_000005.10:g.157753923_157753933dup
GRCh37.p13 chr 5	NC_000005.9:g.157180940_157180941del
GRCh37.p13 chr 5	NC_000005.9:g.157180941del
GRCh37.p13 chr 5	NC_000005.9:g.157180941dup
GRCh37.p13 chr 5	NC_000005.9:g.157180940_157180941dup
GRCh37.p13 chr 5	NC_000005.9:g.157180936_157180941dup
GRCh37.p13 chr 5	NC_000005.9:g.157180931_157180941dup

Gene: LSM11, LSM11, U7 small nuclear RNA associated (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LSM11 transcript	NM_173491.4:c.589-72_589-… NM_173491.4:c.589-72_589-71del	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)₁₁=	delTT	delT	dupT	dupTT	dup(T)₆	dup(T)₁₁
GRCh38.p14 chr 5	NC_000005.10:g.157753923_157753933=	NC_000005.10:g.157753932_157753933del	NC_000005.10:g.157753933del	NC_000005.10:g.157753933dup	NC_000005.10:g.157753932_157753933dup	NC_000005.10:g.157753928_157753933dup	NC_000005.10:g.157753923_157753933dup
GRCh37.p13 chr 5	NC_000005.9:g.157180931_157180941=	NC_000005.9:g.157180940_157180941del	NC_000005.9:g.157180941del	NC_000005.9:g.157180941dup	NC_000005.9:g.157180940_157180941dup	NC_000005.9:g.157180936_157180941dup	NC_000005.9:g.157180931_157180941dup
LSM11 transcript	NM_173491.2:c.589-81=	NM_173491.2:c.589-72_589-71del	NM_173491.2:c.589-71del	NM_173491.2:c.589-71dup	NM_173491.2:c.589-72_589-71dup	NM_173491.2:c.589-76_589-71dup	NM_173491.2:c.589-81_589-71dup
LSM11 transcript	NM_173491.4:c.589-81=	NM_173491.4:c.589-72_589-71del	NM_173491.4:c.589-71del	NM_173491.4:c.589-71dup	NM_173491.4:c.589-72_589-71dup	NM_173491.4:c.589-76_589-71dup	NM_173491.4:c.589-81_589-71dup

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#.

67 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42580480	Mar 14, 2006 (126)
2	HGSV	ss80033124	Dec 03, 2013 (138)
3	HGSV	ss81802255	Dec 04, 2013 (138)
4	HUMANGENOME_JCVI	ss95411650	Feb 06, 2009 (130)
5	HUMANGENOME_JCVI	ss98684609	Mar 15, 2016 (147)
6	BUSHMAN	ss193832238	Jul 04, 2010 (132)
7	GMI	ss287783589	May 09, 2011 (134)
8	GMI	ss288668328	May 04, 2012 (137)
9	PJP	ss295252570	May 09, 2011 (134)
10	PJP	ss295252571	May 09, 2011 (137)
11	TISHKOFF	ss554233848	Apr 25, 2013 (138)
12	SSMP	ss663574653	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666333793	Apr 25, 2013 (138)
14	1000GENOMES	ss1374730918	Jan 10, 2018 (151)
15	1000GENOMES	ss1374730919	Aug 21, 2014 (142)
16	1000GENOMES	ss1374730920	Aug 21, 2014 (142)
17	EVA_UK10K_ALSPAC	ss1704938041	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1704938102	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1710239444	Apr 01, 2015 (144)
20	EVA_UK10K_ALSPAC	ss1710239447	Apr 01, 2015 (144)
21	SYSTEMSBIOZJU	ss2626184477	Nov 08, 2017 (151)
22	SWEGEN	ss2998085031	Nov 08, 2017 (151)
23	BEROUKHIMLAB	ss3644198652	Oct 12, 2018 (152)
24	BIOINF_KMB_FNS_UNIBA	ss3645917063	Oct 12, 2018 (152)
25	BIOINF_KMB_FNS_UNIBA	ss3645917064	Oct 12, 2018 (152)
26	EVA_DECODE	ss3716057539	Jul 13, 2019 (153)
27	EVA_DECODE	ss3716057540	Jul 13, 2019 (153)
28	EVA_DECODE	ss3716057541	Jul 13, 2019 (153)
29	EVA_DECODE	ss3716057542	Jul 13, 2019 (153)
30	EVA_DECODE	ss3716057543	Jul 13, 2019 (153)
31	ACPOP	ss3732971643	Jul 13, 2019 (153)
32	ACPOP	ss3732971644	Jul 13, 2019 (153)
33	PACBIO	ss3785299575	Jul 13, 2019 (153)
34	PACBIO	ss3790674858	Jul 13, 2019 (153)
35	PACBIO	ss3795551958	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3807454941	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3807454942	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3807454943	Jul 13, 2019 (153)
39	KHV_HUMAN_GENOMES	ss3807454944	Jul 13, 2019 (153)
40	EVA	ss3829594492	Apr 26, 2020 (154)
41	EVA	ss3838270695	Apr 26, 2020 (154)
42	EVA	ss3843714144	Apr 26, 2020 (154)
43	KOGIC	ss3957993626	Apr 26, 2020 (154)
44	KOGIC	ss3957993627	Apr 26, 2020 (154)
45	FSA-LAB	ss3984322114	Apr 26, 2021 (155)
46	FSA-LAB	ss3984322115	Apr 26, 2021 (155)
47	GNOMAD	ss4132543269	Apr 26, 2021 (155)
48	GNOMAD	ss4132543270	Apr 26, 2021 (155)
49	GNOMAD	ss4132543271	Apr 26, 2021 (155)
50	GNOMAD	ss4132543272	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5174966215	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5174966216	Apr 26, 2021 (155)
53	EVA	ss5237188096	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5266479948	Oct 13, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5266479949	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5464379792	Oct 13, 2022 (156)
57	HUGCELL_USP	ss5464379793	Oct 13, 2022 (156)
58	EVA	ss5624152217	Oct 13, 2022 (156)
59	EVA	ss5624152218	Oct 13, 2022 (156)
60	TOMMO_GENOMICS	ss5712282501	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5712282502	Oct 13, 2022 (156)
62	EVA	ss5800125454	Oct 13, 2022 (156)
63	YY_MCH	ss5806921282	Oct 13, 2022 (156)
64	EVA	ss5835890154	Oct 13, 2022 (156)
65	EVA	ss5835890155	Oct 13, 2022 (156)
66	EVA	ss5855090938	Oct 13, 2022 (156)
67	EVA	ss5980325801	Oct 13, 2022 (156)
68	1000Genomes	NC_000005.9 - 157180931	Oct 12, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16501999 (NC_000005.9:157180930:T: 1023/3854) Row 16502000 (NC_000005.9:157180930::T 407/3854)	-	Oct 12, 2018 (152)
70	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16501999 (NC_000005.9:157180930:T: 1023/3854) Row 16502000 (NC_000005.9:157180930::T 407/3854)	-	Oct 12, 2018 (152)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 209695618 (NC_000005.10:157753922::T 14552/136802) Row 209695619 (NC_000005.10:157753922::TT 2/136872) Row 209695620 (NC_000005.10:157753922:T: 48837/136704)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 209695618 (NC_000005.10:157753922::T 14552/136802) Row 209695619 (NC_000005.10:157753922::TT 2/136872) Row 209695620 (NC_000005.10:157753922:T: 48837/136704)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 209695618 (NC_000005.10:157753922::T 14552/136802) Row 209695619 (NC_000005.10:157753922::TT 2/136872) Row 209695620 (NC_000005.10:157753922:T: 48837/136704)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 209695618 (NC_000005.10:157753922::T 14552/136802) Row 209695619 (NC_000005.10:157753922::TT 2/136872) Row 209695620 (NC_000005.10:157753922:T: 48837/136704)...	-	Apr 26, 2021 (155)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 14371627 (NC_000005.10:157753922:T: 965/1832) Row 14371628 (NC_000005.10:157753923::T 11/1832)	-	Apr 26, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 14371627 (NC_000005.10:157753922:T: 965/1832) Row 14371628 (NC_000005.10:157753923::T 11/1832)	-	Apr 26, 2020 (154)
77	Northern Sweden Submission ignored due to conflicting rows: Row 6256508 (NC_000005.9:157180930:T: 217/594) Row 6256509 (NC_000005.9:157180930::T 56/594)	-	Jul 13, 2019 (153)
78	Northern Sweden Submission ignored due to conflicting rows: Row 6256508 (NC_000005.9:157180930:T: 217/594) Row 6256509 (NC_000005.9:157180930::T 56/594)	-	Jul 13, 2019 (153)
79	8.3KJPN Submission ignored due to conflicting rows: Row 32935522 (NC_000005.9:157180930:T: 8994/16760) Row 32935523 (NC_000005.9:157180930::T 180/16760)	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 32935522 (NC_000005.9:157180930:T: 8994/16760) Row 32935523 (NC_000005.9:157180930::T 180/16760)	-	Apr 26, 2021 (155)
81	14KJPN Submission ignored due to conflicting rows: Row 46119605 (NC_000005.10:157753922:T: 15073/28258) Row 46119606 (NC_000005.10:157753922::T 298/28258)	-	Oct 13, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 46119605 (NC_000005.10:157753922:T: 15073/28258) Row 46119606 (NC_000005.10:157753922::T 298/28258)	-	Oct 13, 2022 (156)
83	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16501999 (NC_000005.9:157180930:T: 920/3708) Row 16502000 (NC_000005.9:157180930::T 418/3708)	-	Oct 12, 2018 (152)
84	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16501999 (NC_000005.9:157180930:T: 920/3708) Row 16502000 (NC_000005.9:157180930::T 418/3708)	-	Oct 12, 2018 (152)
85	ALFA	NC_000005.10 - 157753923	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)
rs371933055	May 13, 2013 (138)
rs67214253	Feb 26, 2009 (130)
rs142822378	May 11, 2012 (137)
rs796245045	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
29649295, ss1374730918, ss3984322115	NC_000005.9:157180930:TT:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTT	(self)
ss3716057539, ss3807454943, ss4132543272	NC_000005.10:157753922:TT:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTT	(self)
2252524429	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTT	(self)
ss288668328, ss295252570	NC_000005.8:157113508:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss295252571	NC_000005.8:157113518:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss663574653, ss1704938041, ss1704938102, ss2626184477, ss2998085031, ss3644198652, ss3732971643, ss3785299575, ss3790674858, ss3795551958, ss3838270695, ss5174966215, ss5624152217, ss5800125454, ss5835890154, ss5980325801	NC_000005.9:157180930:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss1374730919	NC_000005.9:157180931:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss554233848	NC_000005.9:157180940:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss3645917064, ss3807454942, ss3843714144, ss3957993626, ss4132543271, ss5237188096, ss5266479948, ss5464379792, ss5712282501, ss5806921282, ss5855090938	NC_000005.10:157753922:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
2252524429	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss3716057540, ss3807454941	NC_000005.10:157753923:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss287783589	NT_023133.13:1992203:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss42580480, ss95411650, ss98684609	NT_023133.13:1992213:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss193832238	NT_023133.14:1992598:T:	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss666333793, ss3732971644, ss3829594492, ss3984322114, ss5174966216, ss5624152218, ss5835890155	NC_000005.9:157180930::T	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1710239444, ss1710239447	NC_000005.9:157180931::T	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1374730920	NC_000005.9:157180932::T	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3645917063, ss4132543269, ss5266479949, ss5464379793, ss5712282502	NC_000005.10:157753922::T	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
2252524429	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3957993627	NC_000005.10:157753923::T	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3716057541, ss3807454944	NC_000005.10:157753924::T	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss98684609	NT_023133.13:1992213:T:TT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss80033124, ss81802255	NT_023133.13:1992214::T	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4132543270	NC_000005.10:157753922::TT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2252524429	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTTT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3716057542	NC_000005.10:157753924::TTTTTT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3716057543	NC_000005.10:157753924::TTTTTTTTTTT	NC_000005.10:157753922:TTTTTTTTTTT… NC_000005.10:157753922:TTTTTTTTTTT: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 rs35074350

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

rs35074350