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rs1060503187

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503187(C;C)
Make rs1060503187(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60822638
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503187
dbSNP (old)rs1060503187
ClinGenrs1060503187
ebirs1060503187
HLIrs1060503187
Exacrs1060503187
Varsomers1060503187
Maprs1060503187
PheGenIrs1060503187
Biobankrs1060503187
1000 genomesrs1060503187
hgdprs1060503187
ensemblrs1060503187
gopubmedrs1060503187
geneviewrs1060503187
scholarrs1060503187
googlers1060503187
pharmgkbrs1060503187
gwascentralrs1060503187
openSNPrs1060503187
23andMers1060503187
23andMe allrs1060503187
SNP Nexus

SNPshotrs1060503187
SNPdbers1060503187
MSV3drs1060503187
GWAS Ctlgrs1060503187
Max Magnitude0
ClinVar
Risk rs1060503187(C;C)
Alt rs1060503187(C;C)
Reference Rs1060503187(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61735197G>C
CLNSRC
CLNACC RCV000464132.1,