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rs1064794718

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position119870778
GeneNDUFA1, RNF113A
is asnp
is mentioned by
dbSNPrs1064794718
dbSNP (classic)rs1064794718
ClinGenrs1064794718
ebirs1064794718
HLIrs1064794718
Exacrs1064794718
Gnomadrs1064794718
Varsomers1064794718
LitVarrs1064794718
Maprs1064794718
PheGenIrs1064794718
Biobankrs1064794718
1000 genomesrs1064794718
hgdprs1064794718
ensemblrs1064794718
geneviewrs1064794718
scholarrs1064794718
googlers1064794718
pharmgkbrs1064794718
gwascentralrs1064794718
openSNPrs1064794718
23andMers1064794718
23andMe allrs1064794718
SNPshotrs1064794718
SNPdbers1064794718
MSV3drs1064794718
GWAS Ctlgrs1064794718
Max Magnitude0
ClinVar
Risk rs1064794718(G;G)
Alt rs1064794718(G;G)
Reference Rs1064794718(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RNF113A NDUFA1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119004741T>C
CLNSRC
CLNACC RCV000485614.1,