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rs796051962

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796051962(-;-)
Make rs796051962(-;GT)
Make rs796051962(GT;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158682322
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051962
ebirs796051962
HLIrs796051962
Exacrs796051962
Varsomers796051962
Maprs796051962
PheGenIrs796051962
hapmaprs796051962
1000 genomesrs796051962
hgdprs796051962
ensemblrs796051962
gopubmedrs796051962
geneviewrs796051962
scholarrs796051962
googlers796051962
pharmgkbrs796051962
gwascentralrs796051962
openSNPrs796051962
23andMers796051962
23andMe allrs796051962
SNP Nexus

SNPshotrs796051962
SNPdbers796051962
MSV3drs796051962
GWAS Ctlgrs796051962
Max Magnitude0
ClinVar
Risk rs796051962(GT;GT)
Alt rs796051962(GT;GT)
Reference rs796051962(;)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159603473_159603474dupGT
CLNSRC
CLNACC RCV000185904.1,