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rs1060503189

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503189(-;-)
Make rs1060503189(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60816502
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503189
dbSNP (old)rs1060503189
ClinGenrs1060503189
ebirs1060503189
HLIrs1060503189
Exacrs1060503189
Gnomadrs1060503189
Varsomers1060503189
Maprs1060503189
PheGenIrs1060503189
Biobankrs1060503189
1000 genomesrs1060503189
hgdprs1060503189
ensemblrs1060503189
gopubmedrs1060503189
geneviewrs1060503189
scholarrs1060503189
googlers1060503189
pharmgkbrs1060503189
gwascentralrs1060503189
openSNPrs1060503189
23andMers1060503189
23andMe allrs1060503189
SNP Nexus

SNPshotrs1060503189
SNPdbers1060503189
MSV3drs1060503189
GWAS Ctlgrs1060503189
Max Magnitude0
ClinVar
Risk rs1060503189(-;-)
Alt rs1060503189(-;-)
Reference Rs1060503189(G;G)
Significance Probable-Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61729061delG
CLNSRC
CLNACC RCV000457698.1,