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rs796051972

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051972(C;G)
Make rs796051972(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26234263
GeneHADHA
is asnp
is mentioned by
dbSNPrs796051972
ebirs796051972
HLIrs796051972
Exacrs796051972
Varsomers796051972
Maprs796051972
PheGenIrs796051972
hapmaprs796051972
1000 genomesrs796051972
hgdprs796051972
ensemblrs796051972
gopubmedrs796051972
geneviewrs796051972
scholarrs796051972
googlers796051972
pharmgkbrs796051972
gwascentralrs796051972
openSNPrs796051972
23andMers796051972
23andMe allrs796051972
SNP Nexus

SNPshotrs796051972
SNPdbers796051972
MSV3drs796051972
GWAS Ctlgrs796051972
Max Magnitude0
ClinVar
Risk rs796051972(G;G)
Alt rs796051972(G;G)
Reference rs796051972(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HADHA
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.26457131G>C
CLNSRC
CLNACC RCV000185937.1,