Name: rs11409165
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.

rs11409165

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:241587752-241587763 (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 / dupT…
delTT / delT / dupT / dupTT / dupTTT
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.01631 (217/13306, ALFA)
dupT=0.2011 (1007/5008, 1000G)
dupT=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KMO : 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	13306	TTTTTTTTTTTT=0.98317	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.01631, TTTTTTTTTTTTTT=0.00053, TTTTTTTTTTTTTTT=0.00000	0.968101	0.000752	0.031147	4
European	Sub	11056	TTTTTTTTTTTT=0.97974	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.01963, TTTTTTTTTTTTTT=0.00063, TTTTTTTTTTTTTTT=0.00000	0.961601	0.000906	0.037493	3
African	Sub	1466	TTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	54	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1412	TTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	56	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	100	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	238	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	66	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	324	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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	13306	(T)₁₂=0.98317	delTT=0.00000, delT=0.00000, dupT=0.01631, dupTT=0.00053, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	11056	(T)₁₂=0.97974	delTT=0.00000, delT=0.00000, dupT=0.01963, dupTT=0.00063, dupTTT=0.00000
Allele Frequency Aggregator	African	Sub	1466	(T)₁₂=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Other	Sub	324	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	238	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	100	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	66	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	56	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.2011
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.2897
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.2202
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.0676
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.158
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.258
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.20

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.241587762_241587763del
GRCh38.p14 chr 1	NC_000001.11:g.241587763del
GRCh38.p14 chr 1	NC_000001.11:g.241587763dup
GRCh38.p14 chr 1	NC_000001.11:g.241587762_241587763dup
GRCh38.p14 chr 1	NC_000001.11:g.241587761_241587763dup
GRCh37.p13 chr 1	NC_000001.10:g.241751064_241751065del
GRCh37.p13 chr 1	NC_000001.10:g.241751065del
GRCh37.p13 chr 1	NC_000001.10:g.241751065dup
GRCh37.p13 chr 1	NC_000001.10:g.241751064_241751065dup
GRCh37.p13 chr 1	NC_000001.10:g.241751063_241751065dup

Gene: KMO, kynurenine 3-monooxygenase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KMO transcript variant 1	NM_003679.5:c.1016-986_10… NM_003679.5:c.1016-986_1016-985del	N/A	Intron Variant
KMO transcript variant X1	XM_005273337.2:c.1016-986… XM_005273337.2:c.1016-986_1016-985del	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	dupTTT
GRCh38.p14 chr 1	NC_000001.11:g.241587752_241587763=	NC_000001.11:g.241587762_241587763del	NC_000001.11:g.241587763del	NC_000001.11:g.241587763dup	NC_000001.11:g.241587762_241587763dup	NC_000001.11:g.241587761_241587763dup
GRCh37.p13 chr 1	NC_000001.10:g.241751054_241751065=	NC_000001.10:g.241751064_241751065del	NC_000001.10:g.241751065del	NC_000001.10:g.241751065dup	NC_000001.10:g.241751064_241751065dup	NC_000001.10:g.241751063_241751065dup
KMO transcript	NM_003679.4:c.1016-996=	NM_003679.4:c.1016-986_1016-985del	NM_003679.4:c.1016-985del	NM_003679.4:c.1016-985dup	NM_003679.4:c.1016-986_1016-985dup	NM_003679.4:c.1016-987_1016-985dup
KMO transcript variant 1	NM_003679.5:c.1016-996=	NM_003679.5:c.1016-986_1016-985del	NM_003679.5:c.1016-985del	NM_003679.5:c.1016-985dup	NM_003679.5:c.1016-986_1016-985dup	NM_003679.5:c.1016-987_1016-985dup
KMO transcript variant X1	XM_005273337.1:c.1136-996=	XM_005273337.1:c.1136-986_1136-985del	XM_005273337.1:c.1136-985del	XM_005273337.1:c.1136-985dup	XM_005273337.1:c.1136-986_1136-985dup	XM_005273337.1:c.1136-987_1136-985dup
KMO transcript variant X1	XM_005273337.2:c.1016-996=	XM_005273337.2:c.1016-986_1016-985del	XM_005273337.2:c.1016-985del	XM_005273337.2:c.1016-985dup	XM_005273337.2:c.1016-986_1016-985dup	XM_005273337.2:c.1016-987_1016-985dup
KMO transcript variant X2	XM_005273338.1:c.773-996=	XM_005273338.1:c.773-986_773-985del	XM_005273338.1:c.773-985del	XM_005273338.1:c.773-985dup	XM_005273338.1:c.773-986_773-985dup	XM_005273338.1:c.773-987_773-985dup

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#.

41 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79940231	Dec 04, 2013 (138)
2	BL	ss255978582	May 09, 2011 (138)
3	GMI	ss288113661	May 04, 2012 (137)
4	PJP	ss294634316	May 09, 2011 (137)
5	SSMP	ss663172596	Apr 01, 2015 (144)
6	1000GENOMES	ss1368063491	Aug 21, 2014 (142)
7	EVA_GENOME_DK	ss1574119608	Apr 01, 2015 (144)
8	JJLAB	ss2030386968	Sep 14, 2016 (149)
9	SYSTEMSBIOZJU	ss2624666680	Nov 08, 2017 (151)
10	SWEGEN	ss2988744141	Nov 08, 2017 (151)
11	MCHAISSO	ss3065359203	Nov 08, 2017 (151)
12	EVA_DECODE	ss3688984829	Jul 12, 2019 (153)
13	EVA_DECODE	ss3688984830	Jul 12, 2019 (153)
14	EVA_DECODE	ss3688984831	Jul 12, 2019 (153)
15	ACPOP	ss3728022962	Jul 12, 2019 (153)
16	ACPOP	ss3728022963	Jul 12, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3800562672	Jul 12, 2019 (153)
18	EVA	ss3826740441	Apr 25, 2020 (154)
19	KOGIC	ss3946854143	Apr 25, 2020 (154)
20	KOGIC	ss3946854144	Apr 25, 2020 (154)
21	GNOMAD	ss4014301103	Apr 25, 2021 (155)
22	GNOMAD	ss4014301104	Apr 25, 2021 (155)
23	GNOMAD	ss4014301105	Apr 25, 2021 (155)
24	GNOMAD	ss4014301106	Apr 25, 2021 (155)
25	GNOMAD	ss4014301107	Apr 25, 2021 (155)
26	TOMMO_GENOMICS	ss5149236693	Apr 25, 2021 (155)
27	TOMMO_GENOMICS	ss5149236694	Apr 25, 2021 (155)
28	TOMMO_GENOMICS	ss5149236695	Apr 25, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5246415024	Oct 17, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5246415025	Oct 17, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5246415026	Oct 17, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5246415027	Oct 17, 2022 (156)
33	HUGCELL_USP	ss5446793903	Oct 17, 2022 (156)
34	HUGCELL_USP	ss5446793904	Oct 17, 2022 (156)
35	HUGCELL_USP	ss5446793905	Oct 17, 2022 (156)
36	HUGCELL_USP	ss5446793906	Oct 17, 2022 (156)
37	TOMMO_GENOMICS	ss5677229482	Oct 17, 2022 (156)
38	TOMMO_GENOMICS	ss5677229483	Oct 17, 2022 (156)
39	TOMMO_GENOMICS	ss5677229484	Oct 17, 2022 (156)
40	YY_MCH	ss5801799467	Oct 17, 2022 (156)
41	EVA	ss5849367855	Oct 17, 2022 (156)
42	1000Genomes	NC_000001.10 - 241751054	Oct 11, 2018 (152)
43	The Danish reference pan genome	NC_000001.10 - 241751054	Apr 25, 2020 (154)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 44605007 (NC_000001.11:241587751::T 19109/134668) Row 44605008 (NC_000001.11:241587751::TT 1692/134860) Row 44605009 (NC_000001.11:241587751::TTT 1/134874)...	-	Apr 25, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 44605007 (NC_000001.11:241587751::T 19109/134668) Row 44605008 (NC_000001.11:241587751::TT 1692/134860) Row 44605009 (NC_000001.11:241587751::TTT 1/134874)...	-	Apr 25, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 44605007 (NC_000001.11:241587751::T 19109/134668) Row 44605008 (NC_000001.11:241587751::TT 1692/134860) Row 44605009 (NC_000001.11:241587751::TTT 1/134874)...	-	Apr 25, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 44605007 (NC_000001.11:241587751::T 19109/134668) Row 44605008 (NC_000001.11:241587751::TT 1692/134860) Row 44605009 (NC_000001.11:241587751::TTT 1/134874)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 44605007 (NC_000001.11:241587751::T 19109/134668) Row 44605008 (NC_000001.11:241587751::TT 1692/134860) Row 44605009 (NC_000001.11:241587751::TTT 1/134874)...	-	Apr 25, 2021 (155)
49	Korean Genome Project Submission ignored due to conflicting rows: Row 3232144 (NC_000001.11:241587752::T 442/1832) Row 3232145 (NC_000001.11:241587751:T: 19/1832)	-	Apr 25, 2020 (154)
50	Korean Genome Project Submission ignored due to conflicting rows: Row 3232144 (NC_000001.11:241587752::T 442/1832) Row 3232145 (NC_000001.11:241587751:T: 19/1832)	-	Apr 25, 2020 (154)
51	Northern Sweden Submission ignored due to conflicting rows: Row 1307827 (NC_000001.10:241751053::T 27/600) Row 1307828 (NC_000001.10:241751053::TT 7/600)	-	Jul 12, 2019 (153)
52	Northern Sweden Submission ignored due to conflicting rows: Row 1307827 (NC_000001.10:241751053::T 27/600) Row 1307828 (NC_000001.10:241751053::TT 7/600)	-	Jul 12, 2019 (153)
53	8.3KJPN Submission ignored due to conflicting rows: Row 7206000 (NC_000001.10:241751053::T 3295/16760) Row 7206001 (NC_000001.10:241751053:T: 13/16760) Row 7206002 (NC_000001.10:241751053::TT 3/16760)	-	Apr 25, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 7206000 (NC_000001.10:241751053::T 3295/16760) Row 7206001 (NC_000001.10:241751053:T: 13/16760) Row 7206002 (NC_000001.10:241751053::TT 3/16760)	-	Apr 25, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 7206000 (NC_000001.10:241751053::T 3295/16760) Row 7206001 (NC_000001.10:241751053:T: 13/16760) Row 7206002 (NC_000001.10:241751053::TT 3/16760)	-	Apr 25, 2021 (155)
56	14KJPN Submission ignored due to conflicting rows: Row 11066586 (NC_000001.11:241587751::T 5523/28256) Row 11066587 (NC_000001.11:241587751:T: 11/28256) Row 11066588 (NC_000001.11:241587751::TT 5/28256)	-	Oct 17, 2022 (156)
57	14KJPN Submission ignored due to conflicting rows: Row 11066586 (NC_000001.11:241587751::T 5523/28256) Row 11066587 (NC_000001.11:241587751:T: 11/28256) Row 11066588 (NC_000001.11:241587751::TT 5/28256)	-	Oct 17, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 11066586 (NC_000001.11:241587751::T 5523/28256) Row 11066587 (NC_000001.11:241587751:T: 11/28256) Row 11066588 (NC_000001.11:241587751::TT 5/28256)	-	Oct 17, 2022 (156)
59	ALFA	NC_000001.11 - 241587752	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).

Associated ID	History Updated (Build)
rs34855269	May 11, 2012 (137)
rs58459435	May 11, 2012 (137)
rs71757690	May 11, 2012 (137)
rs72314779	May 11, 2012 (137)
rs138821557	May 15, 2013 (138)
rs143580478	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4014301107, ss5246415027, ss5446793906	NC_000001.11:241587751:TT:	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTT	(self)
12376525296	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss2988744141, ss5149236694	NC_000001.10:241751053:T:	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3688984829, ss3946854144, ss4014301106, ss5246415026, ss5446793905, ss5677229483	NC_000001.11:241587751:T:	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
12376525296	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss255978582	NC_000001.9:239817676::T	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss294634316	NC_000001.9:239817683::T	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss288113661	NC_000001.9:239817688::T	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6235530, 211284, ss663172596, ss1368063491, ss1574119608, ss2030386968, ss2624666680, ss3728022962, ss3826740441, ss5149236693	NC_000001.10:241751053::T	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3065359203, ss3800562672, ss4014301103, ss5246415024, ss5446793903, ss5677229482, ss5801799467, ss5849367855	NC_000001.11:241587751::T	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12376525296	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3688984830, ss3946854143	NC_000001.11:241587752::T	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss79940231	NT_167186.1:35268844::T	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3728022963, ss5149236695	NC_000001.10:241751053::TT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4014301104, ss5246415025, ss5446793904, ss5677229484	NC_000001.11:241587751::TT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12376525296	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3688984831	NC_000001.11:241587752::TT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4014301105	NC_000001.11:241587751::TTT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12376525296	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:241587751:TTTTTTTTTTT… NC_000001.11:241587751:TTTTTTTTTTTT: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 rs11409165

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

rs11409165