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rs267607101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607101(C;T)
Make rs267607101(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position149378537
GeneTAB2
is asnp
is mentioned by
dbSNPrs267607101
ebirs267607101
HLIrs267607101
Exacrs267607101
Varsomers267607101
Maprs267607101
PheGenIrs267607101
hapmaprs267607101
1000 genomesrs267607101
hgdprs267607101
ensemblrs267607101
gopubmedrs267607101
geneviewrs267607101
scholarrs267607101
googlers267607101
pharmgkbrs267607101
gwascentralrs267607101
openSNPrs267607101
23andMers267607101
23andMe allrs267607101
SNP Nexus

SNPshotrs267607101
SNPdbers267607101
MSV3drs267607101
GWAS Ctlgrs267607101
Max Magnitude0
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,