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rs796051961

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051961(C;C)
Make rs796051961(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158680608
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051961
ebirs796051961
HLIrs796051961
Exacrs796051961
Varsomers796051961
Maprs796051961
PheGenIrs796051961
hapmaprs796051961
1000 genomesrs796051961
hgdprs796051961
ensemblrs796051961
gopubmedrs796051961
geneviewrs796051961
scholarrs796051961
googlers796051961
pharmgkbrs796051961
gwascentralrs796051961
openSNPrs796051961
23andMers796051961
23andMe allrs796051961
SNP Nexus

SNPshotrs796051961
SNPdbers796051961
MSV3drs796051961
GWAS Ctlgrs796051961
Max Magnitude0
ClinVar
Risk rs796051961(C;C)
Alt rs796051961(C;C)
Reference rs796051961(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159601760G>C
CLNSRC
CLNACC RCV000185903.1,