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rs1060503188

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503188(C;T)
Make rs1060503188(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60856592
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503188
dbSNP (old)rs1060503188
ClinGenrs1060503188
ebirs1060503188
HLIrs1060503188
Exacrs1060503188
Gnomadrs1060503188
Varsomers1060503188
Maprs1060503188
PheGenIrs1060503188
Biobankrs1060503188
1000 genomesrs1060503188
hgdprs1060503188
ensemblrs1060503188
gopubmedrs1060503188
geneviewrs1060503188
scholarrs1060503188
googlers1060503188
pharmgkbrs1060503188
gwascentralrs1060503188
openSNPrs1060503188
23andMers1060503188
23andMe allrs1060503188
SNPshotrs1060503188
SNPdbers1060503188
MSV3drs1060503188
GWAS Ctlgrs1060503188
Max Magnitude0
ClinVar
Risk rs1060503188(T;T)
Alt rs1060503188(T;T)
Reference Rs1060503188(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61769151C>T
CLNSRC
CLNACC RCV000469838.1,