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rs1064797373

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position68119333
GeneOPHN1
is asnp
is mentioned by
dbSNPrs1064797373
dbSNP (old)rs1064797373
ClinGenrs1064797373
ebirs1064797373
HLIrs1064797373
Exacrs1064797373
Gnomadrs1064797373
Varsomers1064797373
Maprs1064797373
PheGenIrs1064797373
Biobankrs1064797373
1000 genomesrs1064797373
hgdprs1064797373
ensemblrs1064797373
gopubmedrs1064797373
geneviewrs1064797373
scholarrs1064797373
googlers1064797373
pharmgkbrs1064797373
gwascentralrs1064797373
openSNPrs1064797373
23andMers1064797373
23andMe allrs1064797373
SNPshotrs1064797373
SNPdbers1064797373
MSV3drs1064797373
GWAS Ctlgrs1064797373
Max Magnitude0
ClinVar
Risk rs1064797373(C;C)
Alt rs1064797373(C;C)
Reference Rs1064797373(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPHN1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.67339175C>G
CLNSRC
CLNACC RCV000487544.1,