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rs796051902

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051902(G;T)
Make rs796051902(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120738549
GeneACADS
is asnp
is mentioned by
dbSNPrs796051902
ebirs796051902
HLIrs796051902
Exacrs796051902
Varsomers796051902
Maprs796051902
PheGenIrs796051902
hapmaprs796051902
1000 genomesrs796051902
hgdprs796051902
ensemblrs796051902
gopubmedrs796051902
geneviewrs796051902
scholarrs796051902
googlers796051902
pharmgkbrs796051902
gwascentralrs796051902
openSNPrs796051902
23andMers796051902
23andMe allrs796051902
SNP Nexus

SNPshotrs796051902
SNPdbers796051902
MSV3drs796051902
GWAS Ctlgrs796051902
Max Magnitude0
ClinVar
Risk rs796051902(T;T)
Alt rs796051902(T;T)
Reference rs796051902(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121176352G>T
CLNSRC
CLNACC RCV000185687.1,