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rs796051958

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051958(A;G)
Make rs796051958(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158697656
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051958
ebirs796051958
HLIrs796051958
Exacrs796051958
Varsomers796051958
Maprs796051958
PheGenIrs796051958
hapmaprs796051958
1000 genomesrs796051958
hgdprs796051958
ensemblrs796051958
gopubmedrs796051958
geneviewrs796051958
scholarrs796051958
googlers796051958
pharmgkbrs796051958
gwascentralrs796051958
openSNPrs796051958
23andMers796051958
23andMe allrs796051958
SNP Nexus

SNPshotrs796051958
SNPdbers796051958
MSV3drs796051958
GWAS Ctlgrs796051958
Max Magnitude0
ClinVar
Risk rs796051958(G;G)
Alt rs796051958(G;G)
Reference rs796051958(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159618808A>G
CLNSRC
CLNACC RCV000185895.2,