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rs1060503180

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503180(C;C)
Make rs1060503180(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60848514
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503180
dbSNP (old)rs1060503180
ClinGenrs1060503180
ebirs1060503180
HLIrs1060503180
Exacrs1060503180
Varsomers1060503180
Maprs1060503180
PheGenIrs1060503180
Biobankrs1060503180
1000 genomesrs1060503180
hgdprs1060503180
ensemblrs1060503180
gopubmedrs1060503180
geneviewrs1060503180
scholarrs1060503180
googlers1060503180
pharmgkbrs1060503180
gwascentralrs1060503180
openSNPrs1060503180
23andMers1060503180
23andMe allrs1060503180
SNP Nexus

SNPshotrs1060503180
SNPdbers1060503180
MSV3drs1060503180
GWAS Ctlgrs1060503180
Max Magnitude0
ClinVar
Risk rs1060503180(C;C)
Alt rs1060503180(C;C)
Reference Rs1060503180(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61761073G>C
CLNSRC
CLNACC RCV000457833.1,