Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793962

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position60838129
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793962
dbSNP (old)rs1064793962
ClinGenrs1064793962
ebirs1064793962
HLIrs1064793962
Exacrs1064793962
Gnomadrs1064793962
Varsomers1064793962
Maprs1064793962
PheGenIrs1064793962
Biobankrs1064793962
1000 genomesrs1064793962
hgdprs1064793962
ensemblrs1064793962
gopubmedrs1064793962
geneviewrs1064793962
scholarrs1064793962
googlers1064793962
pharmgkbrs1064793962
gwascentralrs1064793962
openSNPrs1064793962
23andMers1064793962
23andMe allrs1064793962
SNP Nexus

SNPshotrs1064793962
SNPdbers1064793962
MSV3drs1064793962
GWAS Ctlgrs1064793962
Max Magnitude0
ClinVar
Risk rs1064793962(G;G)
Alt rs1064793962(G;G)
Reference Rs1064793962(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61750688T>G
CLNSRC
CLNACC RCV000480102.1,