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rs1064795031

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position68192970
GeneOPHN1
is asnp
is mentioned by
dbSNPrs1064795031
dbSNP (old)rs1064795031
ClinGenrs1064795031
ebirs1064795031
HLIrs1064795031
Exacrs1064795031
Gnomadrs1064795031
Varsomers1064795031
LitVarrs1064795031
Maprs1064795031
PheGenIrs1064795031
Biobankrs1064795031
1000 genomesrs1064795031
hgdprs1064795031
ensemblrs1064795031
gopubmedrs1064795031
geneviewrs1064795031
scholarrs1064795031
googlers1064795031
pharmgkbrs1064795031
gwascentralrs1064795031
openSNPrs1064795031
23andMers1064795031
23andMe allrs1064795031
SNPshotrs1064795031
SNPdbers1064795031
MSV3drs1064795031
GWAS Ctlgrs1064795031
Max Magnitude0
ClinVar
Risk rs1064795031(T;T)
Alt rs1064795031(T;T)
Reference Rs1064795031(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPHN1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.67412812G>A
CLNSRC
CLNACC RCV000481229.1,