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rs1064795757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position6592701
GeneCHD4
is asnp
is mentioned by
dbSNPrs1064795757
dbSNP (old)rs1064795757
ClinGenrs1064795757
ebirs1064795757
HLIrs1064795757
Exacrs1064795757
Gnomadrs1064795757
Varsomers1064795757
Maprs1064795757
PheGenIrs1064795757
Biobankrs1064795757
1000 genomesrs1064795757
hgdprs1064795757
ensemblrs1064795757
gopubmedrs1064795757
geneviewrs1064795757
scholarrs1064795757
googlers1064795757
pharmgkbrs1064795757
gwascentralrs1064795757
openSNPrs1064795757
23andMers1064795757
23andMe allrs1064795757
SNPshotrs1064795757
SNPdbers1064795757
MSV3drs1064795757
GWAS Ctlgrs1064795757
Max Magnitude0
ClinVar
Risk rs1064795757(C;C)
Alt rs1064795757(C;C)
Reference Rs1064795757(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD4
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.6701867C>G
CLNSRC
CLNACC RCV000482594.1,