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rs1060503185

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1060503185(-;-)
Make rs1060503185(-;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60852888
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503185
dbSNP (classic)rs1060503185
ClinGenrs1060503185
ebirs1060503185
HLIrs1060503185
Exacrs1060503185
Gnomadrs1060503185
Varsomers1060503185
LitVarrs1060503185
Maprs1060503185
PheGenIrs1060503185
Biobankrs1060503185
1000 genomesrs1060503185
hgdprs1060503185
ensemblrs1060503185
geneviewrs1060503185
scholarrs1060503185
googlers1060503185
pharmgkbrs1060503185
gwascentralrs1060503185
openSNPrs1060503185
23andMers1060503185
23andMe allrs1060503185
SNPshotrs1060503185
SNPdbers1060503185
MSV3drs1060503185
GWAS Ctlgrs1060503185
Max Magnitude0
ClinVar
Risk rs1060503185(-;-)
Alt rs1060503185(-;-)
Reference Rs1060503185(CT;CT)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61765447_61765448delCT
CLNSRC
CLNACC RCV000475738.1,