SNP Links for Gene (Select 83439) - SNP

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Select item 14915704861.

rs1491570486 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 2:85152438 (GRCh38)
2:85379562 (GRCh37)
Canonical SPDI:: NC_000002.12:85152438::C
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00059/7 (ALFA)
C=0.000806/106 (GnomAD)
C=0.000956/16 (TOMMO)
HGVS:: NC_000002.12:g.85152438_85152439insC, NC_000002.11:g.85379561_85379562insC, NW_025791763.1:g.78624_78625insC

Select item 14915561332.

rs1491556133 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCCC [Show Flanks]
Chromosome:: 2:85308444 (GRCh38)
2:85535568 (GRCh37)
Canonical SPDI:: NC_000002.12:85308444:C:CCCCC
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CCCCC=0.00008/1 (ALFA)
CCCC=0.00006/2 (GnomAD)
HGVS:: NC_000002.12:g.85308445_85308446insCCCC, NC_000002.11:g.85535568_85535569insCCCC, NW_025791763.1:g.234631_234632insCCCC

Select item 14915137813.

rs1491513781 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->GCACACACACACACACACACACACACAC
Chromosome:: no mapping
Canonical SPDI:

Select item 14914730104.

rs1491473010 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 2:85282843 (GRCh38)
2:85509966 (GRCh37)
Canonical SPDI:: NC_000002.12:85282842:TT:
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000085/11 (GnomAD)
HGVS:: NC_000002.12:g.85282843_85282844del, NC_000002.11:g.85509966_85509967del, NW_025791763.1:g.209029_209030del

Select item 14914540225.

rs1491454022 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: 2:85204881 (GRCh38)
2:85432005 (GRCh37)
Canonical SPDI:: NC_000002.12:85204881:T:TGT
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: TG=0.0005/2 (Estonian)
HGVS:: NC_000002.12:g.85204882_85204883insGT, NC_000002.11:g.85432005_85432006insGT, NG_045095.1:g.57_58insGT, NW_025791763.1:g.131068_131069insGT

Select item 14914121706.

rs1491412170 has merged into rs66697146 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:85153352 (GRCh38)
2:85380475 (GRCh37)
Canonical SPDI:: NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85153340:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.85153352_85153359del, NC_000002.12:g.85153353_85153359del, NC_000002.12:g.85153356_85153359del, NC_000002.12:g.85153357_85153359del, NC_000002.12:g.85153358_85153359del, NC_000002.12:g.85153359del, NC_000002.12:g.85153359dup, NC_000002.12:g.85153358_85153359dup, NC_000002.12:g.85153357_85153359dup, NC_000002.12:g.85153356_85153359dup, NC_000002.12:g.85153355_85153359dup, NC_000002.12:g.85153354_85153359dup, NC_000002.12:g.85153353_85153359dup, NC_000002.12:g.85153352_85153359dup, NC_000002.12:g.85153351_85153359dup, NC_000002.12:g.85153350_85153359dup, NC_000002.12:g.85153349_85153359dup, NC_000002.12:g.85153348_85153359dup, NC_000002.12:g.85153347_85153359dup, NC_000002.12:g.85153346_85153359dup, NC_000002.12:g.85153345_85153359dup, NC_000002.12:g.85153344_85153359dup, NC_000002.12:g.85153343_85153359dup, NC_000002.12:g.85153342_85153359dup, NC_000002.12:g.85153341_85153359dup, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.85153359_85153360insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380475_85380482del, NC_000002.11:g.85380476_85380482del, NC_000002.11:g.85380479_85380482del, NC_000002.11:g.85380480_85380482del, NC_000002.11:g.85380481_85380482del, NC_000002.11:g.85380482del, NC_000002.11:g.85380482dup, NC_000002.11:g.85380481_85380482dup, NC_000002.11:g.85380480_85380482dup, NC_000002.11:g.85380479_85380482dup, NC_000002.11:g.85380478_85380482dup, NC_000002.11:g.85380477_85380482dup, NC_000002.11:g.85380476_85380482dup, NC_000002.11:g.85380475_85380482dup, NC_000002.11:g.85380474_85380482dup, NC_000002.11:g.85380473_85380482dup, NC_000002.11:g.85380472_85380482dup, NC_000002.11:g.85380471_85380482dup, NC_000002.11:g.85380470_85380482dup, NC_000002.11:g.85380469_85380482dup, NC_000002.11:g.85380468_85380482dup, NC_000002.11:g.85380467_85380482dup, NC_000002.11:g.85380466_85380482dup, NC_000002.11:g.85380465_85380482dup, NC_000002.11:g.85380464_85380482dup, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.85380482_85380483insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79538_79545del, NW_025791763.1:g.79539_79545del, NW_025791763.1:g.79542_79545del, NW_025791763.1:g.79543_79545del, NW_025791763.1:g.79544_79545del, NW_025791763.1:g.79545del, NW_025791763.1:g.79545dup, NW_025791763.1:g.79544_79545dup, NW_025791763.1:g.79543_79545dup, NW_025791763.1:g.79542_79545dup, NW_025791763.1:g.79541_79545dup, NW_025791763.1:g.79540_79545dup, NW_025791763.1:g.79539_79545dup, NW_025791763.1:g.79538_79545dup, NW_025791763.1:g.79537_79545dup, NW_025791763.1:g.79536_79545dup, NW_025791763.1:g.79535_79545dup, NW_025791763.1:g.79534_79545dup, NW_025791763.1:g.79533_79545dup, NW_025791763.1:g.79532_79545dup, NW_025791763.1:g.79531_79545dup, NW_025791763.1:g.79530_79545dup, NW_025791763.1:g.79529_79545dup, NW_025791763.1:g.79528_79545dup, NW_025791763.1:g.79527_79545dup, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791763.1:g.79545_79546insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913997397.

rs1491399739 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 2:85148791 (GRCh38)
2:85375914 (GRCh37)
Canonical SPDI:: NC_000002.12:85148790:TG:
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000002.12:g.85148791_85148792del, NC_000002.11:g.85375914_85375915del, NW_025791763.1:g.74977_74978del

Select item 14913893338.

rs1491389333 [Homo sapiens]

Variant type:: DELINS
Alleles:: AC>- [Show Flanks]
Chromosome:: 2:85204306 (GRCh38)
2:85431429 (GRCh37)
Canonical SPDI:: NC_000002.12:85204304:CAC:C
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00008/1 (ALFA)
-=0.00007/1 (TOMMO)
HGVS:: NC_000002.12:g.85204306_85204307del, NC_000002.11:g.85431429_85431430del, NW_025791763.1:g.130492_130493del

Select item 14913628219.

rs1491362821 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 2:85298481 (GRCh38)
2:85525604 (GRCh37)
Canonical SPDI:: NC_000002.12:85298480:CA:
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00025/3 (ALFA)
HGVS:: NC_000002.12:g.85298481_85298482del, NC_000002.11:g.85525604_85525605del, NW_025791763.1:g.224667_224668del

Select item 149136150010.

rs1491361500 has merged into rs775849544 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 2:85298490 (GRCh38)
2:85525613 (GRCh37)
Canonical SPDI:: NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:85298481:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.35/14 (GENOME_DK)
HGVS:: NC_000002.12:g.85298490_85298502del, NC_000002.12:g.85298491_85298502del, NC_000002.12:g.85298492_85298502del, NC_000002.12:g.85298493_85298502del, NC_000002.12:g.85298494_85298502del, NC_000002.12:g.85298499_85298502del, NC_000002.12:g.85298500_85298502del, NC_000002.12:g.85298501_85298502del, NC_000002.12:g.85298502del, NC_000002.12:g.85298502dup, NC_000002.12:g.85298501_85298502dup, NC_000002.12:g.85298500_85298502dup, NC_000002.12:g.85298499_85298502dup, NC_000002.12:g.85298498_85298502dup, NC_000002.12:g.85298497_85298502dup, NC_000002.12:g.85298496_85298502dup, NC_000002.12:g.85298495_85298502dup, NC_000002.11:g.85525613_85525625del, NC_000002.11:g.85525614_85525625del, NC_000002.11:g.85525615_85525625del, NC_000002.11:g.85525616_85525625del, NC_000002.11:g.85525617_85525625del, NC_000002.11:g.85525622_85525625del, NC_000002.11:g.85525623_85525625del, NC_000002.11:g.85525624_85525625del, NC_000002.11:g.85525625del, NC_000002.11:g.85525625dup, NC_000002.11:g.85525624_85525625dup, NC_000002.11:g.85525623_85525625dup, NC_000002.11:g.85525622_85525625dup, NC_000002.11:g.85525621_85525625dup, NC_000002.11:g.85525620_85525625dup, NC_000002.11:g.85525619_85525625dup, NC_000002.11:g.85525618_85525625dup, NW_025791763.1:g.224676_224688del, NW_025791763.1:g.224677_224688del, NW_025791763.1:g.224678_224688del, NW_025791763.1:g.224679_224688del, NW_025791763.1:g.224680_224688del, NW_025791763.1:g.224685_224688del, NW_025791763.1:g.224686_224688del, NW_025791763.1:g.224687_224688del, NW_025791763.1:g.224688del, NW_025791763.1:g.224688dup, NW_025791763.1:g.224687_224688dup, NW_025791763.1:g.224686_224688dup, NW_025791763.1:g.224685_224688dup, NW_025791763.1:g.224684_224688dup, NW_025791763.1:g.224683_224688dup, NW_025791763.1:g.224682_224688dup, NW_025791763.1:g.224681_224688dup

Select item 149135919011.

rs1491359190 [Homo sapiens]

Variant type:: INS
Alleles:: ->ACC,GCCCC,GG,GGG,GGGG,GGGGG,TC,TCA,TCC,TCCCCCC,TCCCCCCC,TCCCCCCCCCC,TCCTC,TTC [Show Flanks]
Chromosome:: 2:85204291 (GRCh38)
2:85431415 (GRCh37)
Canonical SPDI:: NC_000002.12:85204291::ACC,NC_000002.12:85204291::GCCCC,NC_000002.12:85204291::GG,NC_000002.12:85204291::GGG,NC_000002.12:85204291::GGGG,NC_000002.12:85204291::GGGGG,NC_000002.12:85204291::TC,NC_000002.12:85204291::TCA,NC_000002.12:85204291::TCC,NC_000002.12:85204291::TCCCCCC,NC_000002.12:85204291::TCCCCCCC,NC_000002.12:85204291::TCCCCCCCCCC,NC_000002.12:85204291::TCCTC,NC_000002.12:85204291::TTC
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGG=0./0 (ALFA)
TCC=0.000004/1 (TOPMED)
GGG=0.002179/61 (TOMMO)
HGVS:: NC_000002.12:g.85204291_85204292insACC, NC_000002.12:g.85204291_85204292insGCCCC, NC_000002.12:g.85204291_85204292insGG, NC_000002.12:g.85204291_85204292insGGG, NC_000002.12:g.85204291_85204292insGGGG, NC_000002.12:g.85204291_85204292insGGGGG, NC_000002.12:g.85204291_85204292insTC, NC_000002.12:g.85204291_85204292insTCA, NC_000002.12:g.85204291_85204292insTCC, NC_000002.12:g.85204291_85204292insTCCCCCC, NC_000002.12:g.85204291_85204292insTCCCCCCC, NC_000002.12:g.85204291_85204292insTCCCCCCCCCC, NC_000002.12:g.85204291_85204292insTCCTC, NC_000002.12:g.85204291_85204292insTTC, NC_000002.11:g.85431414_85431415insACC, NC_000002.11:g.85431414_85431415insGCCCC, NC_000002.11:g.85431414_85431415insGG, NC_000002.11:g.85431414_85431415insGGG, NC_000002.11:g.85431414_85431415insGGGG, NC_000002.11:g.85431414_85431415insGGGGG, NC_000002.11:g.85431414_85431415insTC, NC_000002.11:g.85431414_85431415insTCA, NC_000002.11:g.85431414_85431415insTCC, NC_000002.11:g.85431414_85431415insTCCCCCC, NC_000002.11:g.85431414_85431415insTCCCCCCC, NC_000002.11:g.85431414_85431415insTCCCCCCCCCC, NC_000002.11:g.85431414_85431415insTCCTC, NC_000002.11:g.85431414_85431415insTTC, NW_025791763.1:g.130477_130478insACC, NW_025791763.1:g.130477_130478insGCCCC, NW_025791763.1:g.130477_130478insGG, NW_025791763.1:g.130477_130478insGGG, NW_025791763.1:g.130477_130478insGGGG, NW_025791763.1:g.130477_130478insGGGGG, NW_025791763.1:g.130477_130478insTC, NW_025791763.1:g.130477_130478insTCA, NW_025791763.1:g.130477_130478insTCC, NW_025791763.1:g.130477_130478insTCCCCCC, NW_025791763.1:g.130477_130478insTCCCCCCC, NW_025791763.1:g.130477_130478insTCCCCCCCCCC, NW_025791763.1:g.130477_130478insTCCTC, NW_025791763.1:g.130477_130478insTTC

Select item 149132697812.

rs1491326978 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 2:85282794 (GRCh38)
2:85509917 (GRCh37)
Canonical SPDI:: NC_000002.12:85282793:TT:
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00008/1 (ALFA)
-=0.00004/2 (GnomAD)
HGVS:: NC_000002.12:g.85282794_85282795del, NC_000002.11:g.85509917_85509918del, NW_025791763.1:g.208980_208981del

Select item 149131095213.

rs1491310952 [Homo sapiens]

Variant type:: INS
Alleles:: ->AT,T [Show Flanks]
Chromosome:: 2:85298502 (GRCh38)
2:85525626 (GRCh37)
Canonical SPDI:: NC_000002.12:85298502::AT,NC_000002.12:85298502::T
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.85298502_85298503insAT, NC_000002.12:g.85298502_85298503insT, NC_000002.11:g.85525625_85525626insAT, NC_000002.11:g.85525625_85525626insT, NW_025791763.1:g.224688_224689insAT, NW_025791763.1:g.224688_224689insT

Select item 149127338314.

rs1491273383 has merged into rs774050758 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:85294040 (GRCh38)
2:85521163 (GRCh37)
Canonical SPDI:: NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:85294026:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
TT=0.1/4 (GENOME_DK)
HGVS:: NC_000002.12:g.85294040_85294054del, NC_000002.12:g.85294041_85294054del, NC_000002.12:g.85294043_85294054del, NC_000002.12:g.85294044_85294054del, NC_000002.12:g.85294045_85294054del, NC_000002.12:g.85294046_85294054del, NC_000002.12:g.85294047_85294054del, NC_000002.12:g.85294048_85294054del, NC_000002.12:g.85294049_85294054del, NC_000002.12:g.85294050_85294054del, NC_000002.12:g.85294051_85294054del, NC_000002.12:g.85294052_85294054del, NC_000002.12:g.85294053_85294054del, NC_000002.12:g.85294054del, NC_000002.12:g.85294054dup, NC_000002.12:g.85294053_85294054dup, NC_000002.12:g.85294052_85294054dup, NC_000002.12:g.85294051_85294054dup, NC_000002.12:g.85294050_85294054dup, NC_000002.12:g.85294049_85294054dup, NC_000002.12:g.85294048_85294054dup, NC_000002.12:g.85294047_85294054dup, NC_000002.12:g.85294046_85294054dup, NC_000002.12:g.85294045_85294054dup, NC_000002.12:g.85294044_85294054dup, NC_000002.12:g.85294043_85294054dup, NC_000002.12:g.85294042_85294054dup, NC_000002.12:g.85294041_85294054dup, NC_000002.12:g.85294040_85294054dup, NC_000002.12:g.85294039_85294054dup, NC_000002.12:g.85294038_85294054dup, NC_000002.12:g.85294037_85294054dup, NC_000002.12:g.85294036_85294054dup, NC_000002.12:g.85294035_85294054dup, NC_000002.12:g.85294034_85294054dup, NC_000002.12:g.85294033_85294054dup, NC_000002.11:g.85521163_85521177del, NC_000002.11:g.85521164_85521177del, NC_000002.11:g.85521166_85521177del, NC_000002.11:g.85521167_85521177del, NC_000002.11:g.85521168_85521177del, NC_000002.11:g.85521169_85521177del, NC_000002.11:g.85521170_85521177del, NC_000002.11:g.85521171_85521177del, NC_000002.11:g.85521172_85521177del, NC_000002.11:g.85521173_85521177del, NC_000002.11:g.85521174_85521177del, NC_000002.11:g.85521175_85521177del, NC_000002.11:g.85521176_85521177del, NC_000002.11:g.85521177del, NC_000002.11:g.85521177dup, NC_000002.11:g.85521176_85521177dup, NC_000002.11:g.85521175_85521177dup, NC_000002.11:g.85521174_85521177dup, NC_000002.11:g.85521173_85521177dup, NC_000002.11:g.85521172_85521177dup, NC_000002.11:g.85521171_85521177dup, NC_000002.11:g.85521170_85521177dup, NC_000002.11:g.85521169_85521177dup, NC_000002.11:g.85521168_85521177dup, NC_000002.11:g.85521167_85521177dup, NC_000002.11:g.85521166_85521177dup, NC_000002.11:g.85521165_85521177dup, NC_000002.11:g.85521164_85521177dup, NC_000002.11:g.85521163_85521177dup, NC_000002.11:g.85521162_85521177dup, NC_000002.11:g.85521161_85521177dup, NC_000002.11:g.85521160_85521177dup, NC_000002.11:g.85521159_85521177dup, NC_000002.11:g.85521158_85521177dup, NC_000002.11:g.85521157_85521177dup, NC_000002.11:g.85521156_85521177dup, NW_025791763.1:g.220226_220240del, NW_025791763.1:g.220227_220240del, NW_025791763.1:g.220229_220240del, NW_025791763.1:g.220230_220240del, NW_025791763.1:g.220231_220240del, NW_025791763.1:g.220232_220240del, NW_025791763.1:g.220233_220240del, NW_025791763.1:g.220234_220240del, NW_025791763.1:g.220235_220240del, NW_025791763.1:g.220236_220240del, NW_025791763.1:g.220237_220240del, NW_025791763.1:g.220238_220240del, NW_025791763.1:g.220239_220240del, NW_025791763.1:g.220240del, NW_025791763.1:g.220240dup, NW_025791763.1:g.220239_220240dup, NW_025791763.1:g.220238_220240dup, NW_025791763.1:g.220237_220240dup, NW_025791763.1:g.220236_220240dup, NW_025791763.1:g.220235_220240dup, NW_025791763.1:g.220234_220240dup, NW_025791763.1:g.220233_220240dup, NW_025791763.1:g.220232_220240dup, NW_025791763.1:g.220231_220240dup, NW_025791763.1:g.220230_220240dup, NW_025791763.1:g.220229_220240dup, NW_025791763.1:g.220228_220240dup, NW_025791763.1:g.220227_220240dup, NW_025791763.1:g.220226_220240dup, NW_025791763.1:g.220225_220240dup, NW_025791763.1:g.220224_220240dup, NW_025791763.1:g.220223_220240dup, NW_025791763.1:g.220222_220240dup, NW_025791763.1:g.220221_220240dup, NW_025791763.1:g.220220_220240dup, NW_025791763.1:g.220219_220240dup

Select item 149126750815.

rs1491267508 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 2:85204291 (GRCh38)
2:85431414 (GRCh37)
Canonical SPDI:: NC_000002.12:85204290:TC:
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00006/2 (GnomAD)
HGVS:: NC_000002.12:g.85204291_85204292del, NC_000002.11:g.85431414_85431415del, NW_025791763.1:g.130477_130478del

Select item 149125845916.

rs1491258459 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->A
Chromosome:: no mapping
Canonical SPDI:

Select item 149125148617.

rs1491251486 has merged into rs61569778 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACACACACACACACACACACAC>-,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC [Show Flanks]
Chromosome:: 2:85299877 (GRCh38)
2:85527000 (GRCh37)
Canonical SPDI:: NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000002.12:85299860:ACACACACACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC
Gene:: TCF7L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACACACAC=0./0 (ALFA)
-=0.25/2 (KOREAN)
HGVS:: NC_000002.12:g.85299861AC[8], NC_000002.12:g.85299861AC[10], NC_000002.12:g.85299861AC[11], NC_000002.12:g.85299861AC[12], NC_000002.12:g.85299861AC[13], NC_000002.12:g.85299861AC[14], NC_000002.12:g.85299861AC[15], NC_000002.12:g.85299861AC[16], NC_000002.12:g.85299861AC[17], NC_000002.12:g.85299861AC[18], NC_000002.12:g.85299861AC[19], NC_000002.12:g.85299861AC[20], NC_000002.12:g.85299861AC[21], NC_000002.12:g.85299861AC[23], NC_000002.12:g.85299861AC[24], NC_000002.12:g.85299861AC[25], NC_000002.12:g.85299861AC[26], NC_000002.12:g.85299861AC[27], NC_000002.12:g.85299861AC[28], NC_000002.12:g.85299861AC[29], NC_000002.12:g.85299861AC[30], NC_000002.12:g.85299861AC[31], NC_000002.12:g.85299861AC[32], NC_000002.12:g.85299861AC[33], NC_000002.12:g.85299861AC[34], NC_000002.12:g.85299861AC[35], NC_000002.12:g.85299861AC[36], NC_000002.12:g.85299861AC[37], NC_000002.12:g.85299861AC[38], NC_000002.12:g.85299861AC[39], NC_000002.12:g.85299861AC[40], NC_000002.12:g.85299861AC[41], NC_000002.12:g.85299861AC[42], NC_000002.12:g.85299861AC[43], NC_000002.12:g.85299861AC[44], NC_000002.12:g.85299861AC[46], NC_000002.11:g.85526984AC[8], NC_000002.11:g.85526984AC[10], NC_000002.11:g.85526984AC[11], NC_000002.11:g.85526984AC[12], NC_000002.11:g.85526984AC[13], NC_000002.11:g.85526984AC[14], NC_000002.11:g.85526984AC[15], NC_000002.11:g.85526984AC[16], NC_000002.11:g.85526984AC[17], NC_000002.11:g.85526984AC[18], NC_000002.11:g.85526984AC[19], NC_000002.11:g.85526984AC[20], NC_000002.11:g.85526984AC[21], NC_000002.11:g.85526984AC[23], NC_000002.11:g.85526984AC[24], NC_000002.11:g.85526984AC[25], NC_000002.11:g.85526984AC[26], NC_000002.11:g.85526984AC[27], NC_000002.11:g.85526984AC[28], NC_000002.11:g.85526984AC[29], NC_000002.11:g.85526984AC[30], NC_000002.11:g.85526984AC[31], NC_000002.11:g.85526984AC[32], NC_000002.11:g.85526984AC[33], NC_000002.11:g.85526984AC[34], NC_000002.11:g.85526984AC[35], NC_000002.11:g.85526984AC[36], NC_000002.11:g.85526984AC[37], NC_000002.11:g.85526984AC[38], NC_000002.11:g.85526984AC[39], NC_000002.11:g.85526984AC[40], NC_000002.11:g.85526984AC[41], NC_000002.11:g.85526984AC[42], NC_000002.11:g.85526984AC[43], NC_000002.11:g.85526984AC[44], NC_000002.11:g.85526984AC[46], NW_025791763.1:g.226047AC[8], NW_025791763.1:g.226047AC[10], NW_025791763.1:g.226047AC[11], NW_025791763.1:g.226047AC[12], NW_025791763.1:g.226047AC[13], NW_025791763.1:g.226047AC[14], NW_025791763.1:g.226047AC[15], NW_025791763.1:g.226047AC[16], NW_025791763.1:g.226047AC[17], NW_025791763.1:g.226047AC[18], NW_025791763.1:g.226047AC[19], NW_025791763.1:g.226047AC[20], NW_025791763.1:g.226047AC[21], NW_025791763.1:g.226047AC[23], NW_025791763.1:g.226047AC[24], NW_025791763.1:g.226047AC[25], NW_025791763.1:g.226047AC[26], NW_025791763.1:g.226047AC[27], NW_025791763.1:g.226047AC[28], NW_025791763.1:g.226047AC[29], NW_025791763.1:g.226047AC[30], NW_025791763.1:g.226047AC[31], NW_025791763.1:g.226047AC[32], NW_025791763.1:g.226047AC[33], NW_025791763.1:g.226047AC[34], NW_025791763.1:g.226047AC[35], NW_025791763.1:g.226047AC[36], NW_025791763.1:g.226047AC[37], NW_025791763.1:g.226047AC[38], NW_025791763.1:g.226047AC[39], NW_025791763.1:g.226047AC[40], NW_025791763.1:g.226047AC[41], NW_025791763.1:g.226047AC[42], NW_025791763.1:g.226047AC[43], NW_025791763.1:g.226047AC[44], NW_025791763.1:g.226047AC[46]

Select item 149121580918.

rs1491215809 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 2:85310497 (GRCh38)
2:85537620 (GRCh37)
Canonical SPDI:: NC_000002.12:85310496:AG:
Gene:: TCF7L1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000071/1 (ALFA)
-=0.000021/3 (GnomAD)
-=0.00003/8 (TOPMED)
-=0.000035/1 (TOMMO)
HGVS:: NC_000002.12:g.85310497_85310498del, NC_000002.11:g.85537620_85537621del, NW_025791763.1:g.236683_236684del

Select item 149120288019.

rs1491202880 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 2:85212089 (GRCh38)
2:85439212 (GRCh37)
Canonical SPDI:: NC_000002.12:85212088:CA:
Gene:: TCF7L1 (Varview), LOC102724579 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000002.12:g.85212089_85212090del, NC_000002.11:g.85439212_85439213del, NW_025791763.1:g.138275_138276del

Select item 149119933720.

rs1491199337 has merged into rs971404957 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>-,GG [Show Flanks]
Chromosome:: 2:85310498 (GRCh38)
2:85537621 (GRCh37)
Canonical SPDI:: NC_000002.12:85310497:GGGG:GGG,NC_000002.12:85310497:GGGG:GGGGG
Gene:: TCF7L1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGG=0./0 (ALFA)
-=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.85310501del, NC_000002.12:g.85310501dup, NC_000002.11:g.85537624del, NC_000002.11:g.85537624dup, NW_025791763.1:g.236687del, NW_025791763.1:g.236687dup

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