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rs150231967

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs150231967(A;A)
Make rs150231967(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position49750849
GeneOGDHL
is asnp
is mentioned by
dbSNPrs150231967
ebirs150231967
HLIrs150231967
Exacrs150231967
Varsomers150231967
Maprs150231967
PheGenIrs150231967
hapmaprs150231967
1000 genomesrs150231967
hgdprs150231967
ensemblrs150231967
gopubmedrs150231967
geneviewrs150231967
scholarrs150231967
googlers150231967
pharmgkbrs150231967
gwascentralrs150231967
openSNPrs150231967
23andMers150231967
23andMe allrs150231967
SNP Nexus

SNPshotrs150231967
SNPdbers150231967
MSV3drs150231967
GWAS Ctlgrs150231967
Max Magnitude0
ClinVar
Risk rs150231967(A;A)
Alt rs150231967(A;A)
Reference rs150231967(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene OGDHL
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000010.10:g.50958895T>A
CLNSRC
CLNACC RCV000210590.1,