Name: rs61135741
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.

rs61135741

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:74733976-74733985 (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=0.05039 (595/11808, ALFA)
delT=0.3792 (1828/4821, 1000G)
delT=0.1371 (561/4092, Estonian) (+ 1 more)
(T)₁₀=0.3160 (579/1832, Korea1K)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TYW3 : Intron Variant
CRYZ : 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	11808	TTTTTTTTTT=0.93301	TTTTTTTT=0.00000, TTTTTTTTT=0.05039, TTTTTTTTTTT=0.01660, TTTTTTTTTTTT=0.00000	0.909473	0.006829	0.083698	28
European	Sub	9782	TTTTTTTTTT=0.9193	TTTTTTTT=0.0000, TTTTTTTTT=0.0607, TTTTTTTTTTT=0.0199, TTTTTTTTTTTT=0.0000	0.890189	0.0083	0.101511	19
African	Sub	1390	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	56	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1334	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	12	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	6	TTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	96	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	226	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	44	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	258	TTTTTTTTTT=0.992	TTTTTTTT=0.000, TTTTTTTTT=0.004, TTTTTTTTTTT=0.004, TTTTTTTTTTTT=0.000	0.992188	0.0	0.007812	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11808	(T)₁₀=0.93301	delTT=0.00000, delT=0.05039, dupT=0.01660, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	9782	(T)₁₀=0.9193	delTT=0.0000, delT=0.0607, dupT=0.0199, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1390	(T)₁₀=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Other	Sub	258	(T)₁₀=0.992	delTT=0.000, delT=0.004, dupT=0.004, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	226	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	96	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	44	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	12	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4821	(T)₁₀=0.6208	delT=0.3792
1000Genomes	African	Sub	1234	(T)₁₀=0.7180	delT=0.2820
1000Genomes	East Asian	Sub	1006	(T)₁₀=0.2913	delT=0.7087
1000Genomes	South Asian	Sub	965	(T)₁₀=0.573	delT=0.427
1000Genomes	Europe	Sub	953	(T)₁₀=0.863	delT=0.137
1000Genomes	American	Sub	663	(T)₁₀=0.662	delT=0.338
Genetic variation in the Estonian population	Estonian	Study-wide	4092	(T)₁₀=0.8629	delT=0.1371
Korean Genome Project	KOREAN	Study-wide	1832	(T)₁₀=0.3160	delT=0.6840

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.74733984_74733985del
GRCh38.p14 chr 1	NC_000001.11:g.74733985del
GRCh38.p14 chr 1	NC_000001.11:g.74733985dup
GRCh38.p14 chr 1	NC_000001.11:g.74733984_74733985dup
GRCh37.p13 chr 1	NC_000001.10:g.75199668_75199669del
GRCh37.p13 chr 1	NC_000001.10:g.75199669del
GRCh37.p13 chr 1	NC_000001.10:g.75199669dup
GRCh37.p13 chr 1	NC_000001.10:g.75199668_75199669dup
CRYZ RefSeqGene	NG_029880.1:g.4432_4433del
CRYZ RefSeqGene	NG_029880.1:g.4433del
CRYZ RefSeqGene	NG_029880.1:g.4433dup
CRYZ RefSeqGene	NG_029880.1:g.4432_4433dup

Gene: TYW3, tRNA-yW synthesizing protein 3 homolog (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TYW3 transcript variant 2	NM_001162916.2:c.174+566_… NM_001162916.2:c.174+566_174+567del	N/A	Intron Variant
TYW3 transcript variant 1	NM_138467.3:c.174+566_174… NM_138467.3:c.174+566_174+567del	N/A	Intron Variant
TYW3 transcript variant 3	NR_027962.2:n.	N/A	Intron Variant
TYW3 transcript variant X1	XM_006710347.3:c.174+566_… XM_006710347.3:c.174+566_174+567del	N/A	Intron Variant

Gene: CRYZ, crystallin zeta (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
CRYZ transcript variant 1	NM_001130042.2:c.	N/A	Upstream Transcript Variant
CRYZ transcript variant 3	NM_001130043.2:c.	N/A	Upstream Transcript Variant
CRYZ transcript variant 4	NM_001134759.2:c.	N/A	Upstream Transcript Variant
CRYZ transcript variant 2	NM_001889.4:c.	N/A	Upstream Transcript Variant
CRYZ transcript variant X1	XM_011540747.3:c.	N/A	Upstream Transcript Variant
CRYZ transcript variant X2	XM_017000367.3:c.	N/A	Upstream Transcript Variant
CRYZ transcript variant X3	XM_047446751.1:c.	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)₁₀=	delTT	delT	dupT	dupTT
GRCh38.p14 chr 1	NC_000001.11:g.74733976_74733985=	NC_000001.11:g.74733984_74733985del	NC_000001.11:g.74733985del	NC_000001.11:g.74733985dup	NC_000001.11:g.74733984_74733985dup
GRCh37.p13 chr 1	NC_000001.10:g.75199660_75199669=	NC_000001.10:g.75199668_75199669del	NC_000001.10:g.75199669del	NC_000001.10:g.75199669dup	NC_000001.10:g.75199668_75199669dup
CRYZ RefSeqGene	NG_029880.1:g.4424_4433=	NG_029880.1:g.4432_4433del	NG_029880.1:g.4433del	NG_029880.1:g.4433dup	NG_029880.1:g.4432_4433dup
TYW3 transcript variant 2	NM_001162916.1:c.174+558=	NM_001162916.1:c.174+566_174+567del	NM_001162916.1:c.174+567del	NM_001162916.1:c.174+567dup	NM_001162916.1:c.174+566_174+567dup
TYW3 transcript variant 2	NM_001162916.2:c.174+558=	NM_001162916.2:c.174+566_174+567del	NM_001162916.2:c.174+567del	NM_001162916.2:c.174+567dup	NM_001162916.2:c.174+566_174+567dup
TYW3 transcript variant 1	NM_138467.2:c.174+558=	NM_138467.2:c.174+566_174+567del	NM_138467.2:c.174+567del	NM_138467.2:c.174+567dup	NM_138467.2:c.174+566_174+567dup
TYW3 transcript variant 1	NM_138467.3:c.174+558=	NM_138467.3:c.174+566_174+567del	NM_138467.3:c.174+567del	NM_138467.3:c.174+567dup	NM_138467.3:c.174+566_174+567dup
TYW3 transcript variant X1	XM_006710347.3:c.174+558=	XM_006710347.3:c.174+566_174+567del	XM_006710347.3:c.174+567del	XM_006710347.3:c.174+567dup	XM_006710347.3:c.174+566_174+567dup

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#.

56 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80533705	Sep 08, 2015 (146)
2	BGI	ss104666109	Dec 01, 2009 (137)
3	GMI	ss154549352	Dec 01, 2009 (137)
4	BUSHMAN	ss193109948	Jul 04, 2010 (137)
5	GMI	ss287997055	May 04, 2012 (137)
6	1000GENOMES	ss326049279	May 09, 2011 (137)
7	1000GENOMES	ss326049878	Jan 10, 2018 (151)
8	1000GENOMES	ss326066364	May 09, 2011 (137)
9	LUNTER	ss550947499	Apr 25, 2013 (138)
10	LUNTER	ss550953234	Apr 25, 2013 (138)
11	LUNTER	ss552777148	Apr 25, 2013 (138)
12	SSMP	ss663204289	Apr 01, 2015 (144)
13	1000GENOMES	ss1367736281	Aug 21, 2014 (142)
14	1000GENOMES	ss1367736282	Aug 21, 2014 (142)
15	DDI	ss1536233753	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1700805580	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1700805586	Apr 01, 2015 (144)
18	EVA_UK10K_ALSPAC	ss1709932904	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1709932918	Apr 01, 2015 (144)
20	SYSTEMSBIOZJU	ss2624397859	Jan 10, 2018 (151)
21	SWEGEN	ss2987030160	Jan 10, 2018 (151)
22	MCHAISSO	ss3063593583	Jan 10, 2018 (151)
23	MCHAISSO	ss3064407978	Jan 10, 2018 (151)
24	MCHAISSO	ss3065309067	Jan 10, 2018 (151)
25	BEROUKHIMLAB	ss3644061584	Oct 11, 2018 (152)
26	BIOINF_KMB_FNS_UNIBA	ss3645050650	Oct 11, 2018 (152)
27	EGCUT_WGS	ss3655105943	Jul 12, 2019 (153)
28	EVA_DECODE	ss3687035619	Jul 12, 2019 (153)
29	EVA_DECODE	ss3687035620	Jul 12, 2019 (153)
30	ACPOP	ss3727164049	Jul 12, 2019 (153)
31	ACPOP	ss3727164050	Jul 12, 2019 (153)
32	PACBIO	ss3783447340	Jul 12, 2019 (153)
33	PACBIO	ss3789099918	Jul 12, 2019 (153)
34	PACBIO	ss3793972664	Jul 12, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3799374694	Jul 12, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3799374695	Jul 12, 2019 (153)
37	EVA	ss3826239944	Apr 25, 2020 (154)
38	EVA	ss3836508365	Apr 25, 2020 (154)
39	EVA	ss3841915202	Apr 25, 2020 (154)
40	KOGIC	ss3944771717	Apr 25, 2020 (154)
41	GNOMAD	ss3996036601	Apr 25, 2021 (155)
42	GNOMAD	ss3996036602	Apr 25, 2021 (155)
43	GNOMAD	ss3996036603	Apr 25, 2021 (155)
44	GNOMAD	ss3996036604	Apr 25, 2021 (155)
45	TOMMO_GENOMICS	ss5144553286	Apr 25, 2021 (155)
46	TOMMO_GENOMICS	ss5144553287	Apr 25, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5242736570	Oct 12, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5242736571	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5443754413	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5443754414	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5669497293	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5669497294	Oct 12, 2022 (156)
53	YY_MCH	ss5800712105	Oct 12, 2022 (156)
54	EVA	ss5832139044	Oct 12, 2022 (156)
55	EVA	ss5832139045	Oct 12, 2022 (156)
56	EVA	ss5848962797	Oct 12, 2022 (156)
57	1000Genomes	NC_000001.10 - 75199660	Oct 11, 2018 (152)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1190071 (NC_000001.10:75199659:T: 439/3854) Row 1190072 (NC_000001.10:75199659::T 213/3854)	-	Oct 11, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1190071 (NC_000001.10:75199659:T: 439/3854) Row 1190072 (NC_000001.10:75199659::T 213/3854)	-	Oct 11, 2018 (152)
60	Genetic variation in the Estonian population	NC_000001.10 - 75199660	Oct 11, 2018 (152)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 15354888 (NC_000001.11:74733975::T 7927/137752) Row 15354889 (NC_000001.11:74733975::TT 1/137792) Row 15354890 (NC_000001.11:74733975:T: 26700/137662)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 15354888 (NC_000001.11:74733975::T 7927/137752) Row 15354889 (NC_000001.11:74733975::TT 1/137792) Row 15354890 (NC_000001.11:74733975:T: 26700/137662)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 15354888 (NC_000001.11:74733975::T 7927/137752) Row 15354889 (NC_000001.11:74733975::TT 1/137792) Row 15354890 (NC_000001.11:74733975:T: 26700/137662)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 15354888 (NC_000001.11:74733975::T 7927/137752) Row 15354889 (NC_000001.11:74733975::TT 1/137792) Row 15354890 (NC_000001.11:74733975:T: 26700/137662)...	-	Apr 25, 2021 (155)
65	Korean Genome Project	NC_000001.11 - 74733976	Apr 25, 2020 (154)
66	Northern Sweden Submission ignored due to conflicting rows: Row 448914 (NC_000001.10:75199659:T: 98/600) Row 448915 (NC_000001.10:75199659::T 24/600)	-	Jul 12, 2019 (153)
67	Northern Sweden Submission ignored due to conflicting rows: Row 448914 (NC_000001.10:75199659:T: 98/600) Row 448915 (NC_000001.10:75199659::T 24/600)	-	Jul 12, 2019 (153)
68	8.3KJPN Submission ignored due to conflicting rows: Row 2522593 (NC_000001.10:75199659:T: 12351/16760) Row 2522594 (NC_000001.10:75199659::T 2/16760)	-	Apr 25, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 2522593 (NC_000001.10:75199659:T: 12351/16760) Row 2522594 (NC_000001.10:75199659::T 2/16760)	-	Apr 25, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 3334397 (NC_000001.11:74733975:T: 20828/28258) Row 3334398 (NC_000001.11:74733975::T 4/28258)	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 3334397 (NC_000001.11:74733975:T: 20828/28258) Row 3334398 (NC_000001.11:74733975::T 4/28258)	-	Oct 12, 2022 (156)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1190071 (NC_000001.10:75199659:T: 416/3708) Row 1190072 (NC_000001.10:75199659::T 191/3708)	-	Oct 11, 2018 (152)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1190071 (NC_000001.10:75199659:T: 416/3708) Row 1190072 (NC_000001.10:75199659::T 191/3708)	-	Oct 11, 2018 (152)
74	ALFA	NC_000001.11 - 74733976	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)
rs66818901	May 11, 2012 (137)
rs66818902	Feb 26, 2009 (130)
rs77759899	May 11, 2012 (137)
rs139493937	May 04, 2012 (137)
rs370251497	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3996036604	NC_000001.11:74733975:TT:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTT	(self)
11572215142	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTT	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTT	(self)
ss80533705	NC_000001.8:74911689:T:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
ss287997055, ss326049279, ss326066364, ss550953234, ss552777148	NC_000001.9:74972247:T:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
2172090, 844191, ss663204289, ss1367736281, ss1536233753, ss1700805580, ss1700805586, ss2624397859, ss2987030160, ss3655105943, ss3727164049, ss3826239944, ss5144553286, ss5832139044	NC_000001.10:75199659:T:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
1149718, ss3063593583, ss3064407978, ss3065309067, ss3645050650, ss3687035619, ss3799374695, ss3944771717, ss3996036603, ss5242736570, ss5443754414, ss5669497293, ss5800712105, ss5848962797	NC_000001.11:74733975:T:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
11572215142	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
ss154549352	NT_032977.9:45171577:T:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
ss104666109	NT_032977.9:45171585:T:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
ss193109948	NT_032977.10:74147987:T:	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTT	(self)
ss326049878, ss550947499	NC_000001.9:74972247::T	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3644061584, ss3727164050, ss3783447340, ss3789099918, ss3793972664, ss3836508365, ss5144553287, ss5832139045	NC_000001.10:75199659::T	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss1367736282, ss1709932904, ss1709932918	NC_000001.10:75199660::T	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3841915202, ss3996036601, ss5242736571, ss5443754413, ss5669497294	NC_000001.11:74733975::T	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTT	(self)
11572215142	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3687035620, ss3799374694	NC_000001.11:74733976::T	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3996036602	NC_000001.11:74733975::TT	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTTT	(self)
11572215142	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975:TTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:74733975:TTTTTTTTTT:T… NC_000001.11:74733975: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 rs61135741

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

rs61135741