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rs796051960

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051960(A;A)
Make rs796051960(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158708482
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051960
ebirs796051960
HLIrs796051960
Exacrs796051960
Varsomers796051960
Maprs796051960
PheGenIrs796051960
hapmaprs796051960
1000 genomesrs796051960
hgdprs796051960
ensemblrs796051960
gopubmedrs796051960
geneviewrs796051960
scholarrs796051960
googlers796051960
pharmgkbrs796051960
gwascentralrs796051960
openSNPrs796051960
23andMers796051960
23andMe allrs796051960
SNP Nexus

SNPshotrs796051960
SNPdbers796051960
MSV3drs796051960
GWAS Ctlgrs796051960
Max Magnitude0
ClinVar
Risk rs796051960(A;A)
Alt rs796051960(A;A)
Reference rs796051960(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159629634G>A
CLNSRC
CLNACC RCV000185901.1,