rs267607101

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs267607101(C;T)

Make rs267607101(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

149378537

Gene

TAB2

is a	snp
is	mentioned by
dbSNP	rs267607101
dbSNP (classic)	rs267607101
ClinGen	rs267607101
ebi	rs267607101
HLI	rs267607101
Exac	rs267607101
Gnomad	rs267607101
Varsome	rs267607101
LitVar	rs267607101
Map	rs267607101
PheGenI	rs267607101
Biobank	rs267607101
1000 genomes	rs267607101
hgdp	rs267607101
ensembl	rs267607101
geneview	rs267607101
scholar	rs267607101
google	rs267607101
pharmgkb	rs267607101
gwascentral	rs267607101
openSNP	rs267607101
23andMe	rs267607101
SNPshot	rs267607101
SNPdbe	rs267607101
MSV3d	rs267607101
GWAS Ctlg	rs267607101

Max Magnitude

0

ClinVar
Risk	rs267607101(T;T)
Alt	rs267607101(T;T)
Reference	Rs267607101(C;C)
Significance	Pathogenic
Disease	Congenital heart defects
Variation	info
Gene	TAB2
CLNDBN	Congenital heart defects, multiple types, 2
Reversed	0
HGVS	NC_000006.11:g.149699673C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005521.3,