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rs797044914

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044914(C;C)
Make rs797044914(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position119873328
GeneNDUFA1, RNF113A
is asnp
is mentioned by
dbSNPrs797044914
ebirs797044914
HLIrs797044914
Exacrs797044914
Varsomers797044914
Maprs797044914
PheGenIrs797044914
hapmaprs797044914
1000 genomesrs797044914
hgdprs797044914
ensemblrs797044914
gopubmedrs797044914
geneviewrs797044914
scholarrs797044914
googlers797044914
pharmgkbrs797044914
gwascentralrs797044914
openSNPrs797044914
23andMers797044914
23andMe allrs797044914
SNP Nexus

SNPshotrs797044914
SNPdbers797044914
MSV3drs797044914
GWAS Ctlgrs797044914
Max Magnitude0
ClinVar
Risk rs797044914(C;C)
Alt rs797044914(C;C)
Reference rs797044914(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RNF113A NDUFA1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.119007291T>C
CLNSRC
CLNACC RCV000190744.1,