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rs1064794837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome15
Position93000643
GeneCHD2
is asnp
is mentioned by
dbSNPrs1064794837
dbSNP (classic)rs1064794837
ClinGenrs1064794837
ebirs1064794837
HLIrs1064794837
Exacrs1064794837
Gnomadrs1064794837
Varsomers1064794837
LitVarrs1064794837
Maprs1064794837
PheGenIrs1064794837
Biobankrs1064794837
1000 genomesrs1064794837
hgdprs1064794837
ensemblrs1064794837
geneviewrs1064794837
scholarrs1064794837
googlers1064794837
pharmgkbrs1064794837
gwascentralrs1064794837
openSNPrs1064794837
23andMers1064794837
23andMe allrs1064794837
SNPshotrs1064794837
SNPdbers1064794837
MSV3drs1064794837
GWAS Ctlgrs1064794837
Max Magnitude0
ClinVar
Risk rs1064794837(T;T)
Alt rs1064794837(T;T)
Reference Rs1064794837(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93543873A>T
CLNSRC
CLNACC RCV000480875.1,