Name: rs11306565
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.

rs11306565

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:168588526-168588537 (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
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.4271 (2732/6396, ALFA)
delT=0.4734 (2231/4713, 1000G)
(T)₁₂=0.3630 (1399/3854, ALSPAC) (+ 4 more)
(T)₁₂=0.3560 (1320/3708, TWINSUK)
(T)₁₂=0.360 (359/998, GoNL)
(T)₁₂=0.369 (220/596, NorthernSweden)
(T)₁₂=0.33 (13/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: EGFEM1P : 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	6396	TTTTTTTTTTTT=0.5729	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.4271, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000	0.415572	0.269856	0.314572	32
European	Sub	5336	TTTTTTTTTTTT=0.4886	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.5114, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000	0.3006	0.323463	0.375937	32
African	Sub	792	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	36	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	756	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	42	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	34	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	20	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	84	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	22	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	100	TTTTTTTTTTTT=0.97	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.03, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	0.94	0.0	0.06	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	6396	(T)₁₂=0.5729	delTT=0.0000, delT=0.4271, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	5336	(T)₁₂=0.4886	delTT=0.0000, delT=0.5114, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	792	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	100	(T)₁₂=0.97	delTT=0.00, delT=0.03, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 2	Sub	84	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	42	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4713	(T)₁₂=0.5266	delT=0.4734
1000Genomes	African	Sub	1057	(T)₁₂=0.7181	delT=0.2819
1000Genomes	Europe	Sub	1006	(T)₁₂=0.3280	delT=0.6720
1000Genomes	East Asian	Sub	1003	(T)₁₂=0.5643	delT=0.4357
1000Genomes	South Asian	Sub	976	(T)₁₂=0.600	delT=0.400
1000Genomes	American	Sub	671	(T)₁₂=0.359	delT=0.641
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₂=0.3630	delT=0.6370
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₂=0.3560	delT=0.6440
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	(T)₁₂=0.360	delT=0.640
Northern Sweden	ACPOP	Study-wide	596	(T)₁₂=0.369	delT=0.631
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₂=0.33	delT=0.68

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 3	NC_000003.12:g.168588536_168588537del
GRCh38.p14 chr 3	NC_000003.12:g.168588537del
GRCh38.p14 chr 3	NC_000003.12:g.168588537dup
GRCh38.p14 chr 3	NC_000003.12:g.168588536_168588537dup
GRCh37.p13 chr 3	NC_000003.11:g.168306324_168306325del
GRCh37.p13 chr 3	NC_000003.11:g.168306325del
GRCh37.p13 chr 3	NC_000003.11:g.168306325dup
GRCh37.p13 chr 3	NC_000003.11:g.168306324_168306325dup

Gene: EGFEM1P, EGF like and EMI domain containing 1, pseudogene (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
EGFEM1P transcript	NR_021485.2: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)₁₂=	delTT	delT	dupT	dupTT
GRCh38.p14 chr 3	NC_000003.12:g.168588526_168588537=	NC_000003.12:g.168588536_168588537del	NC_000003.12:g.168588537del	NC_000003.12:g.168588537dup	NC_000003.12:g.168588536_168588537dup
GRCh37.p13 chr 3	NC_000003.11:g.168306314_168306325=	NC_000003.11:g.168306324_168306325del	NC_000003.11:g.168306325del	NC_000003.11:g.168306325dup	NC_000003.11:g.168306324_168306325dup

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#.

55 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DEVINE_LAB	ss15183186	Mar 15, 2016 (147)
2	ABI	ss41999962	Dec 03, 2013 (138)
3	ABI	ss42082351	Dec 03, 2013 (138)
4	HGSV	ss80756269	Sep 08, 2015 (146)
5	HGSV	ss81686252	Sep 08, 2015 (146)
6	HUMANGENOME_JCVI	ss95338243	Feb 05, 2009 (130)
7	BL	ss256033229	May 09, 2011 (137)
8	GMI	ss287738115	May 09, 2011 (137)
9	GMI	ss288446829	May 04, 2012 (137)
10	PJP	ss295138457	May 09, 2011 (137)
11	PJP	ss295138458	May 09, 2011 (134)
12	SSMP	ss663377509	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666235766	Apr 25, 2013 (138)
14	EVA-GONL	ss979433452	Aug 21, 2014 (142)
15	1000GENOMES	ss1371320147	Aug 21, 2014 (142)
16	1000GENOMES	ss1371320150	Aug 21, 2014 (142)
17	DDI	ss1536382605	Apr 01, 2015 (144)
18	EVA_GENOME_DK	ss1576089775	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1703924686	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1703924697	Apr 01, 2015 (144)
21	HAMMER_LAB	ss1800405809	Sep 08, 2015 (146)
22	SWEGEN	ss2993609656	Nov 08, 2017 (151)
23	MCHAISSO	ss3064940683	Nov 08, 2017 (151)
24	BEROUKHIMLAB	ss3644141140	Oct 12, 2018 (152)
25	BIOINF_KMB_FNS_UNIBA	ss3645758129	Oct 12, 2018 (152)
26	URBANLAB	ss3647582515	Oct 12, 2018 (152)
27	EVA_DECODE	ss3710786412	Jul 13, 2019 (153)
28	EVA_DECODE	ss3710786413	Jul 13, 2019 (153)
29	ACPOP	ss3730575787	Jul 13, 2019 (153)
30	PACBIO	ss3784531945	Jul 13, 2019 (153)
31	PACBIO	ss3784531946	Jul 13, 2019 (153)
32	PACBIO	ss3790014860	Jul 13, 2019 (153)
33	PACBIO	ss3794889508	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3804145630	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3804145631	Jul 13, 2019 (153)
36	EVA	ss3828207310	Apr 25, 2020 (154)
37	EVA	ss3842969169	Apr 25, 2020 (154)
38	GNOMAD	ss4085337065	Apr 26, 2021 (155)
39	GNOMAD	ss4085337066	Apr 26, 2021 (155)
40	GNOMAD	ss4085337067	Apr 26, 2021 (155)
41	GNOMAD	ss4085337068	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5162746964	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5162746965	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5256926933	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5256926934	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5256926935	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5455979540	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5455979541	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5695957779	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5695957780	Oct 12, 2022 (156)
51	YY_MCH	ss5804472539	Oct 12, 2022 (156)
52	EVA	ss5826828397	Oct 12, 2022 (156)
53	EVA	ss5853949842	Oct 12, 2022 (156)
54	EVA	ss5872037351	Oct 12, 2022 (156)
55	EVA	ss5962080919	Oct 12, 2022 (156)
56	1000Genomes	NC_000003.11 - 168306314	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children	NC_000003.11 - 168306314	Oct 12, 2018 (152)
58	The Danish reference pan genome	NC_000003.11 - 168306314	Apr 25, 2020 (154)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 131374554 (NC_000003.12:168588525::T 8241/136098) Row 131374555 (NC_000003.12:168588525::TT 7/136178) Row 131374556 (NC_000003.12:168588525:T: 71379/136040)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 131374554 (NC_000003.12:168588525::T 8241/136098) Row 131374555 (NC_000003.12:168588525::TT 7/136178) Row 131374556 (NC_000003.12:168588525:T: 71379/136040)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 131374554 (NC_000003.12:168588525::T 8241/136098) Row 131374555 (NC_000003.12:168588525::TT 7/136178) Row 131374556 (NC_000003.12:168588525:T: 71379/136040)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 131374554 (NC_000003.12:168588525::T 8241/136098) Row 131374555 (NC_000003.12:168588525::TT 7/136178) Row 131374556 (NC_000003.12:168588525:T: 71379/136040)...	-	Apr 26, 2021 (155)
63	Genome of the Netherlands Release 5	NC_000003.11 - 168306314	Apr 25, 2020 (154)
64	Northern Sweden	NC_000003.11 - 168306314	Jul 13, 2019 (153)
65	8.3KJPN Submission ignored due to conflicting rows: Row 20716271 (NC_000003.11:168306313:T: 6742/16760) Row 20716272 (NC_000003.11:168306313::T 7/16760)	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 20716271 (NC_000003.11:168306313:T: 6742/16760) Row 20716272 (NC_000003.11:168306313::T 7/16760)	-	Apr 26, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 29794883 (NC_000003.12:168588525:T: 11337/28258) Row 29794884 (NC_000003.12:168588525::T 16/28258)	-	Oct 12, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 29794883 (NC_000003.12:168588525:T: 11337/28258) Row 29794884 (NC_000003.12:168588525::T 16/28258)	-	Oct 12, 2022 (156)
69	UK 10K study - Twins	NC_000003.11 - 168306314	Oct 12, 2018 (152)
70	ALFA	NC_000003.12 - 168588526	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)
rs34277172	May 11, 2012 (137)
rs34995772	May 23, 2006 (127)
rs59902589	May 25, 2008 (130)
rs72340062	May 11, 2012 (137)
rs140352452	May 11, 2012 (137)
rs146877172	May 04, 2012 (137)
rs368665649	May 13, 2013 (138)
rs869078742	Jul 19, 2016 (147)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3784531945	NC_000003.11:168306313:TT:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3710786412, ss4085337068, ss5256926935	NC_000003.12:168588525:TT:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTT	(self)
11719816986	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTT	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss80756269, ss81686252	NC_000003.9:169789026:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss256033229, ss288446829, ss295138457	NC_000003.10:169789007:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss295138458	NC_000003.10:169789018:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
18492463, 10302508, 872256, 4528381, 3860652, 10302508, ss663377509, ss666235766, ss979433452, ss1371320147, ss1536382605, ss1576089775, ss1703924686, ss1703924697, ss1800405809, ss2993609656, ss3644141140, ss3730575787, ss3784531946, ss3790014860, ss3794889508, ss3828207310, ss5162746964, ss5826828397, ss5962080919	NC_000003.11:168306313:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3064940683, ss3645758129, ss3647582515, ss3804145630, ss3842969169, ss4085337067, ss5256926933, ss5455979540, ss5695957779, ss5804472539, ss5853949842, ss5872037351	NC_000003.12:168588525:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
11719816986	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3710786413	NC_000003.12:168588526:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss287738115	NT_005612.16:74801459:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss42082351	NT_005612.16:74801469:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss15183186, ss41999962, ss95338243	NT_005612.16:74801470:T:	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5162746965	NC_000003.11:168306313::T	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss1371320150	NC_000003.11:168306314::T	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4085337065, ss5256926934, ss5455979541, ss5695957780	NC_000003.12:168588525::T	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11719816986	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3804145631	NC_000003.12:168588526::T	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4085337066	NC_000003.12:168588525::TT	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11719816986	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000003.12:168588525:TTTTTTTTTTT… NC_000003.12:168588525:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(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 rs11306565

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

rs11306565