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rs796051904

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051904(C;C)
Make rs796051904(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120739167
GeneACADS
is asnp
is mentioned by
dbSNPrs796051904
ebirs796051904
HLIrs796051904
Exacrs796051904
Varsomers796051904
Maprs796051904
PheGenIrs796051904
hapmaprs796051904
1000 genomesrs796051904
hgdprs796051904
ensemblrs796051904
gopubmedrs796051904
geneviewrs796051904
scholarrs796051904
googlers796051904
pharmgkbrs796051904
gwascentralrs796051904
openSNPrs796051904
23andMers796051904
23andMe allrs796051904
SNP Nexus

SNPshotrs796051904
SNPdbers796051904
MSV3drs796051904
GWAS Ctlgrs796051904
Max Magnitude0
ClinVar
Risk rs796051904(C;C)
Alt rs796051904(C;C)
Reference rs796051904(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121176970T>C
CLNSRC
CLNACC RCV000185692.1,