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rs1060503181

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060503181(-;-)
Make rs1060503181(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60816456
GeneCHD7
is asnp
is mentioned by
dbSNPrs1060503181
dbSNP (old)rs1060503181
ClinGenrs1060503181
ebirs1060503181
HLIrs1060503181
Exacrs1060503181
Gnomadrs1060503181
Varsomers1060503181
Maprs1060503181
PheGenIrs1060503181
Biobankrs1060503181
1000 genomesrs1060503181
hgdprs1060503181
ensemblrs1060503181
gopubmedrs1060503181
geneviewrs1060503181
scholarrs1060503181
googlers1060503181
pharmgkbrs1060503181
gwascentralrs1060503181
openSNPrs1060503181
23andMers1060503181
23andMe allrs1060503181
SNPshotrs1060503181
SNPdbers1060503181
MSV3drs1060503181
GWAS Ctlgrs1060503181
Max Magnitude0
ClinVar
Risk rs1060503181(-;-)
Alt rs1060503181(-;-)
Reference Rs1060503181(T;T)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61729015delT
CLNSRC
CLNACC RCV000464453.1,