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rs1060503184

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060503184(-;-)
Make rs1060503184(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60742490
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503184
dbSNP (classic)rs1060503184
ClinGenrs1060503184
ebirs1060503184
HLIrs1060503184
Exacrs1060503184
Gnomadrs1060503184
Varsomers1060503184
LitVarrs1060503184
Maprs1060503184
PheGenIrs1060503184
Biobankrs1060503184
1000 genomesrs1060503184
hgdprs1060503184
ensemblrs1060503184
geneviewrs1060503184
scholarrs1060503184
googlers1060503184
pharmgkbrs1060503184
gwascentralrs1060503184
openSNPrs1060503184
23andMers1060503184
23andMe allrs1060503184
SNPshotrs1060503184
SNPdbers1060503184
MSV3drs1060503184
GWAS Ctlgrs1060503184
Max Magnitude0
ClinVar
Risk rs1060503184(-;-)
Alt rs1060503184(-;-)
Reference Rs1060503184(T;T)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61655049delT
CLNSRC
CLNACC RCV000467254.1,