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rs1060503183

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060503183(G;G)
Make rs1060503183(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60823837
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503183
dbSNP (old)rs1060503183
ClinGenrs1060503183
ebirs1060503183
HLIrs1060503183
Exacrs1060503183
Gnomadrs1060503183
Varsomers1060503183
Maprs1060503183
PheGenIrs1060503183
Biobankrs1060503183
1000 genomesrs1060503183
hgdprs1060503183
ensemblrs1060503183
gopubmedrs1060503183
geneviewrs1060503183
scholarrs1060503183
googlers1060503183
pharmgkbrs1060503183
gwascentralrs1060503183
openSNPrs1060503183
23andMers1060503183
23andMe allrs1060503183
SNP Nexus

SNPshotrs1060503183
SNPdbers1060503183
MSV3drs1060503183
GWAS Ctlgrs1060503183
Max Magnitude0
ClinVar
Risk rs1060503183(G;G)
Alt rs1060503183(G;G)
Reference Rs1060503183(T;T)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61736396T>G
CLNSRC
CLNACC RCV000460607.1,