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rs1060503182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503182(C;C)
Make rs1060503182(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60794985
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503182
ClinGenrs1060503182
ebirs1060503182
HLIrs1060503182
Exacrs1060503182
Varsomers1060503182
Maprs1060503182
PheGenIrs1060503182
Biobankrs1060503182
1000 genomesrs1060503182
hgdprs1060503182
ensemblrs1060503182
gopubmedrs1060503182
geneviewrs1060503182
scholarrs1060503182
googlers1060503182
pharmgkbrs1060503182
gwascentralrs1060503182
openSNPrs1060503182
23andMers1060503182
23andMe allrs1060503182
SNP Nexus

SNPshotrs1060503182
SNPdbers1060503182
MSV3drs1060503182
GWAS Ctlgrs1060503182
Max Magnitude0
ClinVar
Risk rs1060503182(C;C)
Alt rs1060503182(C;C)
Reference Rs1060503182(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61707544G>C
CLNSRC
CLNACC RCV000468880.1,