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rs796051905

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051905(G;T)
Make rs796051905(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120739321
GeneACADS
is asnp
is mentioned by
dbSNPrs796051905
ebirs796051905
HLIrs796051905
Exacrs796051905
Varsomers796051905
Maprs796051905
PheGenIrs796051905
hapmaprs796051905
1000 genomesrs796051905
hgdprs796051905
ensemblrs796051905
gopubmedrs796051905
geneviewrs796051905
scholarrs796051905
googlers796051905
pharmgkbrs796051905
gwascentralrs796051905
openSNPrs796051905
23andMers796051905
23andMe allrs796051905
SNP Nexus

SNPshotrs796051905
SNPdbers796051905
MSV3drs796051905
GWAS Ctlgrs796051905
Max Magnitude0
ClinVar
Risk rs796051905(T;T)
Alt rs796051905(T;T)
Reference rs796051905(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121177124G>T
CLNSRC
CLNACC RCV000185697.1,