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rs796051966

From SNPedia

Orientationplus
Geno Mag Summary
(TGT;TGT) 0 common in clinvar
Make rs796051966(-;-)
Make rs796051966(-;TGT)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158682232
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051966
ebirs796051966
HLIrs796051966
Exacrs796051966
Varsomers796051966
Maprs796051966
PheGenIrs796051966
hapmaprs796051966
1000 genomesrs796051966
hgdprs796051966
ensemblrs796051966
gopubmedrs796051966
geneviewrs796051966
scholarrs796051966
googlers796051966
pharmgkbrs796051966
gwascentralrs796051966
openSNPrs796051966
23andMers796051966
23andMe allrs796051966
SNP Nexus

SNPshotrs796051966
SNPdbers796051966
MSV3drs796051966
GWAS Ctlgrs796051966
Max Magnitude0
ClinVar
Risk rs796051966(;)
Alt rs796051966(;)
Reference rs796051966(TGT;TGT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159603384_159603386delTGT
CLNSRC
CLNACC RCV000185908.1,