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rs796051959

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051959(A;A)
Make rs796051959(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158699087
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051959
ebirs796051959
HLIrs796051959
Exacrs796051959
Varsomers796051959
Maprs796051959
PheGenIrs796051959
hapmaprs796051959
1000 genomesrs796051959
hgdprs796051959
ensemblrs796051959
gopubmedrs796051959
geneviewrs796051959
scholarrs796051959
googlers796051959
pharmgkbrs796051959
gwascentralrs796051959
openSNPrs796051959
23andMers796051959
23andMe allrs796051959
SNP Nexus

SNPshotrs796051959
SNPdbers796051959
MSV3drs796051959
GWAS Ctlgrs796051959
Max Magnitude0
ClinVar
Risk rs796051959(A;A)
Alt rs796051959(A;A)
Reference rs796051959(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159620239G>A
CLNSRC
CLNACC RCV000185897.1,