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rs796051965

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051965(A;T)
Make rs796051965(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158682427
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051965
ebirs796051965
HLIrs796051965
Exacrs796051965
Varsomers796051965
Maprs796051965
PheGenIrs796051965
hapmaprs796051965
1000 genomesrs796051965
hgdprs796051965
ensemblrs796051965
gopubmedrs796051965
geneviewrs796051965
scholarrs796051965
googlers796051965
pharmgkbrs796051965
gwascentralrs796051965
openSNPrs796051965
23andMers796051965
23andMe allrs796051965
SNP Nexus

SNPshotrs796051965
SNPdbers796051965
MSV3drs796051965
GWAS Ctlgrs796051965
Max Magnitude0
ClinVar
Risk rs796051965(T;T)
Alt rs796051965(T;T)
Reference Rs796051965(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159603579A>T
CLNSRC
CLNACC RCV000185907.2,