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rs875989879

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989879(C;T)
Make rs875989879(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position60853017
GeneCHD7
is asnp
is mentioned by
dbSNPrs875989879
ebirs875989879
HLIrs875989879
Exacrs875989879
Varsomers875989879
Maprs875989879
PheGenIrs875989879
hapmaprs875989879
1000 genomesrs875989879
hgdprs875989879
ensemblrs875989879
gopubmedrs875989879
geneviewrs875989879
scholarrs875989879
googlers875989879
pharmgkbrs875989879
gwascentralrs875989879
openSNPrs875989879
23andMers875989879
23andMe allrs875989879
SNP Nexus

SNPshotrs875989879
SNPdbers875989879
MSV3drs875989879
GWAS Ctlgrs875989879
Max Magnitude0
ClinVar
Risk rs875989879(T;T)
Alt rs875989879(T;T)
Reference rs875989879(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61765576C>T
CLNSRC University Hospital of Geneva
CLNACC RCV000211558.1,