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rs1064793755

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position68299098
GeneOPHN1
is asnp
is mentioned by
dbSNPrs1064793755
dbSNP (old)rs1064793755
ClinGenrs1064793755
ebirs1064793755
HLIrs1064793755
Exacrs1064793755
Gnomadrs1064793755
Varsomers1064793755
Maprs1064793755
PheGenIrs1064793755
Biobankrs1064793755
1000 genomesrs1064793755
hgdprs1064793755
ensemblrs1064793755
gopubmedrs1064793755
geneviewrs1064793755
scholarrs1064793755
googlers1064793755
pharmgkbrs1064793755
gwascentralrs1064793755
openSNPrs1064793755
23andMers1064793755
23andMe allrs1064793755
SNPshotrs1064793755
SNPdbers1064793755
MSV3drs1064793755
GWAS Ctlgrs1064793755
Max Magnitude0
ClinVar
Risk rs1064793755(C;C)
Alt rs1064793755(C;C)
Reference Rs1064793755(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OPHN1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.67518940T>G
CLNSRC
CLNACC RCV000481065.1,