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rs267606724

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606724(C;T)
Make rs267606724(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position60841997
GeneCHD7
is asnp
is mentioned by
dbSNPrs267606724
ebirs267606724
HLIrs267606724
Exacrs267606724
Varsomers267606724
Maprs267606724
PheGenIrs267606724
hapmaprs267606724
1000 genomesrs267606724
hgdprs267606724
ensemblrs267606724
gopubmedrs267606724
geneviewrs267606724
scholarrs267606724
googlers267606724
pharmgkbrs267606724
gwascentralrs267606724
openSNPrs267606724
23andMers267606724
23andMe allrs267606724
SNP Nexus

SNPshotrs267606724
SNPdbers267606724
MSV3drs267606724
GWAS Ctlgrs267606724
Max Magnitude0
ClinVar
Risk rs267606724(G,T;G,T)
Alt rs267606724(G,T;G,T)
Reference rs267606724(C;C)
Significance Pathogenic
Disease CHARGE association not provided
Variation info
Gene CHD7
CLNDBN CHARGE association not provided
Reversed 0
HGVS NC_000008.10:g.61754556C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002118.2, RCV000122607.1,