Name: rs35305882
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.

rs35305882

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:124463222-124463231 (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
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₀=0.302554 (80083/264690, TOPMED)
(T)₁₀=0.3812 (2955/7752, ALFA)
(T)₁₀=0.2933 (1469/5008, 1000G) (+ 5 more)
(T)₁₀=0.2792 (1251/4480, Estonian)
(T)₁₀=0.2551 (983/3854, ALSPAC)
(T)₁₀=0.2721 (1009/3708, TWINSUK)
(T)₁₀=0.227 (136/600, NorthernSweden)
(T)₁₀=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LHPP : 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	7752	TTTTTTTTTT=0.3812	TTTTTTTT=0.0000, TTTTTTTTT=0.6188, TTTTTTTTTTT=0.0000	0.206914	0.44453	0.348555	32
European	Sub	7102	TTTTTTTTTT=0.3354	TTTTTTTT=0.0000, TTTTTTTTT=0.6646, TTTTTTTTTTT=0.0000	0.149254	0.478457	0.372289	32
African	Sub	484	TTTTTTTTTT=0.903	TTTTTTTT=0.000, TTTTTTTTT=0.097, TTTTTTTTTTT=0.000	0.859504	0.053719	0.086777	33
African Others	Sub	26	TTTTTTTTTT=0.88	TTTTTTTT=0.00, TTTTTTTTT=0.12, TTTTTTTTTTT=0.00	0.769231	0.0	0.230769	0
African American	Sub	458	TTTTTTTTTT=0.904	TTTTTTTT=0.000, TTTTTTTTT=0.096, TTTTTTTTTTT=0.000	0.864629	0.056769	0.078603	35
Asian	Sub	4	TTTTTTTTTT=0.0	TTTTTTTT=0.0, TTTTTTTTT=1.0, TTTTTTTTTTT=0.0	0.0	1.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTT=0.0	TTTTTTTT=0.0, TTTTTTTTT=1.0, TTTTTTTTTTT=0.0	0.0	1.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTT=0.0	TTTTTTTT=0.0, TTTTTTTTT=1.0, TTTTTTTTTTT=0.0	0.0	1.0	0.0	N/A
Latin American 1	Sub	16	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	64	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	TTTTTTTTTT=0.86	TTTTTTTT=0.00, TTTTTTTTT=0.14, TTTTTTTTTTT=0.00	0.714286	0.0	0.285714	0
Other	Sub	68	TTTTTTTTTT=0.65	TTTTTTTT=0.00, TTTTTTTTT=0.35, TTTTTTTTTTT=0.00	0.558824	0.264706	0.176471	7

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
TopMed	Global	Study-wide	264690	(T)₁₀=0.302554	delT=0.697446
Allele Frequency Aggregator	Total	Global	7752	(T)₁₀=0.3812	delTT=0.0000, delT=0.6188, dupT=0.0000
Allele Frequency Aggregator	European	Sub	7102	(T)₁₀=0.3354	delTT=0.0000, delT=0.6646, dupT=0.0000
Allele Frequency Aggregator	African	Sub	484	(T)₁₀=0.903	delTT=0.000, delT=0.097, dupT=0.000
Allele Frequency Aggregator	Other	Sub	68	(T)₁₀=0.65	delTT=0.00, delT=0.35, dupT=0.00
Allele Frequency Aggregator	Latin American 2	Sub	64	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(T)₁₀=0.86	delTT=0.00, delT=0.14, dupT=0.00
Allele Frequency Aggregator	Asian	Sub	4	(T)₁₀=0.0	delTT=0.0, delT=1.0, dupT=0.0
1000Genomes	Global	Study-wide	5008	(T)₁₀=0.2933	delT=0.7067
1000Genomes	African	Sub	1322	(T)₁₀=0.3820	delT=0.6180
1000Genomes	East Asian	Sub	1008	(T)₁₀=0.1310	delT=0.8690
1000Genomes	Europe	Sub	1006	(T)₁₀=0.2893	delT=0.7107
1000Genomes	South Asian	Sub	978	(T)₁₀=0.336	delT=0.664
1000Genomes	American	Sub	694	(T)₁₀=0.305	delT=0.695
Genetic variation in the Estonian population	Estonian	Study-wide	4480	(T)₁₀=0.2792	delT=0.7208
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₀=0.2551	delT=0.7449
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₀=0.2721	delT=0.7279
Northern Sweden	ACPOP	Study-wide	600	(T)₁₀=0.227	delT=0.773
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₀=0.20	delT=0.80

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 10	NC_000010.11:g.124463229_124463231del
GRCh38.p14 chr 10	NC_000010.11:g.124463230_124463231del
GRCh38.p14 chr 10	NC_000010.11:g.124463231del
GRCh38.p14 chr 10	NC_000010.11:g.124463231dup
GRCh38.p14 chr 10	NC_000010.11:g.124463230_124463231dup
GRCh37.p13 chr 10	NC_000010.10:g.126151798_126151800del
GRCh37.p13 chr 10	NC_000010.10:g.126151799_126151800del
GRCh37.p13 chr 10	NC_000010.10:g.126151800del
GRCh37.p13 chr 10	NC_000010.10:g.126151800dup
GRCh37.p13 chr 10	NC_000010.10:g.126151799_126151800dup

Gene: LHPP, phospholysine phosphohistidine inorganic pyrophosphate phosphatase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LHPP transcript variant 2	NM_001167880.2:c.125+1242… NM_001167880.2:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant 3	NM_001318331.2:c.125+1242… NM_001318331.2:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant 4	NM_001318332.2:c.125+1242… NM_001318332.2:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant 1	NM_022126.4:c.125+1242_12… NM_022126.4:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant X2	XM_005270026.4:c.125+1242… XM_005270026.4:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant X4	XM_011540058.4:c.125+1242… XM_011540058.4:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant X1	XM_017016509.2:c.125+1242… XM_017016509.2:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant X3	XM_024448122.1:c.125+1242… XM_024448122.1:c.125+1242_125+1244del	N/A	Intron Variant
LHPP transcript variant X6	XM_017016512.2:c.	N/A	Genic Upstream Transcript Variant
LHPP transcript variant X5	XR_001747177.3: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)₁₀=	delTTT	delTT	delT	dupT	dupTT
GRCh38.p14 chr 10	NC_000010.11:g.124463222_124463231=	NC_000010.11:g.124463229_124463231del	NC_000010.11:g.124463230_124463231del	NC_000010.11:g.124463231del	NC_000010.11:g.124463231dup	NC_000010.11:g.124463230_124463231dup
GRCh37.p13 chr 10	NC_000010.10:g.126151791_126151800=	NC_000010.10:g.126151798_126151800del	NC_000010.10:g.126151799_126151800del	NC_000010.10:g.126151800del	NC_000010.10:g.126151800dup	NC_000010.10:g.126151799_126151800dup
LHPP transcript variant 2	NM_001167880.1:c.125+1235=	NM_001167880.1:c.125+1242_125+1244del	NM_001167880.1:c.125+1243_125+1244del	NM_001167880.1:c.125+1244del	NM_001167880.1:c.125+1244dup	NM_001167880.1:c.125+1243_125+1244dup
LHPP transcript variant 2	NM_001167880.2:c.125+1235=	NM_001167880.2:c.125+1242_125+1244del	NM_001167880.2:c.125+1243_125+1244del	NM_001167880.2:c.125+1244del	NM_001167880.2:c.125+1244dup	NM_001167880.2:c.125+1243_125+1244dup
LHPP transcript variant 3	NM_001318331.2:c.125+1235=	NM_001318331.2:c.125+1242_125+1244del	NM_001318331.2:c.125+1243_125+1244del	NM_001318331.2:c.125+1244del	NM_001318331.2:c.125+1244dup	NM_001318331.2:c.125+1243_125+1244dup
LHPP transcript variant 4	NM_001318332.2:c.125+1235=	NM_001318332.2:c.125+1242_125+1244del	NM_001318332.2:c.125+1243_125+1244del	NM_001318332.2:c.125+1244del	NM_001318332.2:c.125+1244dup	NM_001318332.2:c.125+1243_125+1244dup
LHPP transcript variant 1	NM_022126.3:c.125+1235=	NM_022126.3:c.125+1242_125+1244del	NM_022126.3:c.125+1243_125+1244del	NM_022126.3:c.125+1244del	NM_022126.3:c.125+1244dup	NM_022126.3:c.125+1243_125+1244dup
LHPP transcript variant 1	NM_022126.4:c.125+1235=	NM_022126.4:c.125+1242_125+1244del	NM_022126.4:c.125+1243_125+1244del	NM_022126.4:c.125+1244del	NM_022126.4:c.125+1244dup	NM_022126.4:c.125+1243_125+1244dup
LHPP transcript variant X1	XM_005270025.1:c.125+1235=	XM_005270025.1:c.125+1242_125+1244del	XM_005270025.1:c.125+1243_125+1244del	XM_005270025.1:c.125+1244del	XM_005270025.1:c.125+1244dup	XM_005270025.1:c.125+1243_125+1244dup
LHPP transcript variant X2	XM_005270026.1:c.125+1235=	XM_005270026.1:c.125+1242_125+1244del	XM_005270026.1:c.125+1243_125+1244del	XM_005270026.1:c.125+1244del	XM_005270026.1:c.125+1244dup	XM_005270026.1:c.125+1243_125+1244dup
LHPP transcript variant X2	XM_005270026.4:c.125+1235=	XM_005270026.4:c.125+1242_125+1244del	XM_005270026.4:c.125+1243_125+1244del	XM_005270026.4:c.125+1244del	XM_005270026.4:c.125+1244dup	XM_005270026.4:c.125+1243_125+1244dup
LHPP transcript variant X3	XM_005270027.1:c.125+1235=	XM_005270027.1:c.125+1242_125+1244del	XM_005270027.1:c.125+1243_125+1244del	XM_005270027.1:c.125+1244del	XM_005270027.1:c.125+1244dup	XM_005270027.1:c.125+1243_125+1244dup
LHPP transcript variant X4	XM_011540058.4:c.125+1235=	XM_011540058.4:c.125+1242_125+1244del	XM_011540058.4:c.125+1243_125+1244del	XM_011540058.4:c.125+1244del	XM_011540058.4:c.125+1244dup	XM_011540058.4:c.125+1243_125+1244dup
LHPP transcript variant X1	XM_017016509.2:c.125+1235=	XM_017016509.2:c.125+1242_125+1244del	XM_017016509.2:c.125+1243_125+1244del	XM_017016509.2:c.125+1244del	XM_017016509.2:c.125+1244dup	XM_017016509.2:c.125+1243_125+1244dup
LHPP transcript variant X3	XM_024448122.1:c.125+1235=	XM_024448122.1:c.125+1242_125+1244del	XM_024448122.1:c.125+1243_125+1244del	XM_024448122.1:c.125+1244del	XM_024448122.1:c.125+1244dup	XM_024448122.1:c.125+1243_125+1244dup

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#.

59 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39783541	Dec 03, 2013 (138)
2	BCMHGSC_JDW	ss103517668	Dec 01, 2009 (131)
3	BGI	ss104679597	Feb 13, 2009 (137)
4	BUSHMAN	ss193209852	Jul 04, 2010 (137)
5	BL	ss256143160	May 09, 2011 (137)
6	GMI	ss287867607	May 09, 2011 (137)
7	GMI	ss289043511	May 04, 2012 (137)
8	1000GENOMES	ss327291324	May 09, 2011 (137)
9	1000GENOMES	ss327374992	May 09, 2011 (137)
10	1000GENOMES	ss327769666	May 09, 2011 (137)
11	LUNTER	ss552079384	Apr 25, 2013 (138)
12	LUNTER	ss552330205	Apr 25, 2013 (138)
13	LUNTER	ss553431651	Apr 25, 2013 (138)
14	SSMP	ss663960438	Apr 01, 2015 (144)
15	BILGI_BIOE	ss666519354	Apr 25, 2013 (138)
16	1000GENOMES	ss1370249778	Aug 21, 2014 (142)
17	DDI	ss1536672940	Apr 01, 2015 (144)
18	EVA_GENOME_DK	ss1574273273	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1706938897	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1706939059	Apr 01, 2015 (144)
21	HAMMER_LAB	ss1806614744	Sep 08, 2015 (146)
22	SYSTEMSBIOZJU	ss2627682772	Nov 08, 2017 (151)
23	SWEGEN	ss3007308339	Nov 08, 2017 (151)
24	MCHAISSO	ss3063673732	Nov 08, 2017 (151)
25	MCHAISSO	ss3064496260	Nov 08, 2017 (151)
26	MCHAISSO	ss3065407984	Nov 08, 2017 (151)
27	BEROUKHIMLAB	ss3644309761	Oct 12, 2018 (152)
28	BIOINF_KMB_FNS_UNIBA	ss3645168835	Oct 12, 2018 (152)
29	URBANLAB	ss3649489734	Oct 12, 2018 (152)
30	EGCUT_WGS	ss3674728248	Jul 13, 2019 (153)
31	EVA_DECODE	ss3690881744	Jul 13, 2019 (153)
32	EVA_DECODE	ss3690881745	Jul 13, 2019 (153)
33	EVA_DECODE	ss3690881746	Jul 13, 2019 (153)
34	ACPOP	ss3737766197	Jul 13, 2019 (153)
35	PACBIO	ss3786815814	Jul 13, 2019 (153)
36	PACBIO	ss3791974043	Jul 13, 2019 (153)
37	PACBIO	ss3796856189	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3814086836	Jul 13, 2019 (153)
39	EVA	ss3832384566	Apr 26, 2020 (154)
40	EVA	ss3839733902	Apr 26, 2020 (154)
41	EVA	ss3845209205	Apr 26, 2020 (154)
42	GNOMAD	ss4227384650	Apr 26, 2021 (155)
43	GNOMAD	ss4227384651	Apr 26, 2021 (155)
44	GNOMAD	ss4227384652	Apr 26, 2021 (155)
45	GNOMAD	ss4227384653	Apr 26, 2021 (155)
46	TOPMED	ss4869900980	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5199919887	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5199919888	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5285818005	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5285818006	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5481206132	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5746427051	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5746427052	Oct 16, 2022 (156)
54	YY_MCH	ss5811973327	Oct 16, 2022 (156)
55	EVA	ss5825096478	Oct 16, 2022 (156)
56	EVA	ss5849786363	Oct 16, 2022 (156)
57	EVA	ss5880937614	Oct 16, 2022 (156)
58	EVA	ss5941605896	Oct 16, 2022 (156)
59	EVA	ss5980645909	Oct 16, 2022 (156)
60	1000Genomes	NC_000010.10 - 126151791	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 126151791	Oct 12, 2018 (152)
62	Genetic variation in the Estonian population	NC_000010.10 - 126151791	Oct 12, 2018 (152)
63	The Danish reference pan genome	NC_000010.10 - 126151791	Apr 26, 2020 (154)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366814805 (NC_000010.11:124463221::T 19/139476) Row 366814806 (NC_000010.11:124463221:T: 97768/139408) Row 366814807 (NC_000010.11:124463221:TT: 20/139476)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366814805 (NC_000010.11:124463221::T 19/139476) Row 366814806 (NC_000010.11:124463221:T: 97768/139408) Row 366814807 (NC_000010.11:124463221:TT: 20/139476)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366814805 (NC_000010.11:124463221::T 19/139476) Row 366814806 (NC_000010.11:124463221:T: 97768/139408) Row 366814807 (NC_000010.11:124463221:TT: 20/139476)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366814805 (NC_000010.11:124463221::T 19/139476) Row 366814806 (NC_000010.11:124463221:T: 97768/139408) Row 366814807 (NC_000010.11:124463221:TT: 20/139476)...	-	Apr 26, 2021 (155)
68	Northern Sweden	NC_000010.10 - 126151791	Jul 13, 2019 (153)
69	8.3KJPN Submission ignored due to conflicting rows: Row 57889194 (NC_000010.10:126151790:T: 14335/16760) Row 57889195 (NC_000010.10:126151790::T 2/16760)	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 57889194 (NC_000010.10:126151790:T: 14335/16760) Row 57889195 (NC_000010.10:126151790::T 2/16760)	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 80264155 (NC_000010.11:124463221:T: 24129/28258) Row 80264156 (NC_000010.11:124463221::T 5/28258)	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 80264155 (NC_000010.11:124463221:T: 24129/28258) Row 80264156 (NC_000010.11:124463221::T 5/28258)	-	Oct 16, 2022 (156)
73	TopMed	NC_000010.11 - 124463222	Apr 26, 2021 (155)
74	UK 10K study - Twins	NC_000010.10 - 126151791	Oct 12, 2018 (152)
75	ALFA	NC_000010.11 - 124463222	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)
rs72511682	May 11, 2012 (137)
rs112829756	May 11, 2012 (137)
rs149617822	May 04, 2012 (137)
rs375538422	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4227384653	NC_000010.11:124463221:TTT:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTT	(self)
ss3690881744, ss4227384652	NC_000010.11:124463221:TT:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTT	(self)
1650978243	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTT	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTT	(self)
ss103517668	NT_030059.13:76956262:TT:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTT	(self)
ss256143160, ss289043511, ss327291324, ss327374992, ss327769666, ss552079384, ss552330205, ss553431651	NC_000010.9:126141780:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
51923077, 28846684, 20466496, 270669, 11051062, 28846684, ss663960438, ss666519354, ss1370249778, ss1536672940, ss1574273273, ss1706938897, ss1706939059, ss1806614744, ss2627682772, ss3007308339, ss3644309761, ss3674728248, ss3737766197, ss3786815814, ss3791974043, ss3796856189, ss3832384566, ss3839733902, ss5199919887, ss5825096478, ss5941605896, ss5980645909	NC_000010.10:126151790:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
85446635, ss3063673732, ss3064496260, ss3065407984, ss3645168835, ss3649489734, ss3814086836, ss3845209205, ss4227384651, ss4869900980, ss5285818005, ss5481206132, ss5746427051, ss5811973327, ss5849786363, ss5880937614	NC_000010.11:124463221:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
1650978243	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
ss3690881745	NC_000010.11:124463222:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
ss287867607	NT_030059.13:76956254:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
ss104679597	NT_030059.13:76956262:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
ss39783541	NT_030059.13:76956263:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
ss193209852	NT_030059.14:82769700:T:	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTT	(self)
ss5199919888	NC_000010.10:126151790::T	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss4227384650, ss5285818006, ss5746427052	NC_000010.11:124463221::T	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTTTT	(self)
1650978243	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTTTT	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3690881746	NC_000010.11:124463223::TT	NC_000010.11:124463221:TTTTTTTTTT:… NC_000010.11:124463221:TTTTTTTTTT:TTTTTTTTTTTT	(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 rs35305882

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

rs35305882