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rs1060499937

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499937(-;-)
Make rs1060499937(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60844998
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060499937
dbSNP (old)rs1060499937
ClinGenrs1060499937
ebirs1060499937
HLIrs1060499937
Exacrs1060499937
Gnomadrs1060499937
Varsomers1060499937
Maprs1060499937
PheGenIrs1060499937
Biobankrs1060499937
1000 genomesrs1060499937
hgdprs1060499937
ensemblrs1060499937
gopubmedrs1060499937
geneviewrs1060499937
scholarrs1060499937
googlers1060499937
pharmgkbrs1060499937
gwascentralrs1060499937
openSNPrs1060499937
23andMers1060499937
23andMe allrs1060499937
SNP Nexus

SNPshotrs1060499937
SNPdbers1060499937
MSV3drs1060499937
GWAS Ctlgrs1060499937
Max Magnitude0
ClinVar
Risk rs1060499937(-;-)
Alt rs1060499937(-;-)
Reference Rs1060499937(G;G)
Significance Probable-Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61757557delG
CLNSRC
CLNACC RCV000456117.1,