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rs1060499560

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499560(-;-)
Make rs1060499560(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60853017
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060499560
dbSNP (old)rs1060499560
ClinGenrs1060499560
ebirs1060499560
HLIrs1060499560
Exacrs1060499560
Gnomadrs1060499560
Varsomers1060499560
Maprs1060499560
PheGenIrs1060499560
Biobankrs1060499560
1000 genomesrs1060499560
hgdprs1060499560
ensemblrs1060499560
gopubmedrs1060499560
geneviewrs1060499560
scholarrs1060499560
googlers1060499560
pharmgkbrs1060499560
gwascentralrs1060499560
openSNPrs1060499560
23andMers1060499560
23andMe allrs1060499560
SNPshotrs1060499560
SNPdbers1060499560
MSV3drs1060499560
GWAS Ctlgrs1060499560
Max Magnitude0
ClinVar
Risk rs1060499560(-;-)
Alt rs1060499560(-;-)
Reference Rs1060499560(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61765576delC
CLNSRC
CLNACC RCV000474707.1,