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rs766183395

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766183395(A;A)
Make rs766183395(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120739366
GeneACADS
is asnp
is mentioned by
dbSNPrs766183395
ebirs766183395
HLIrs766183395
Exacrs766183395
Varsomers766183395
Maprs766183395
PheGenIrs766183395
hapmaprs766183395
1000 genomesrs766183395
hgdprs766183395
ensemblrs766183395
gopubmedrs766183395
geneviewrs766183395
scholarrs766183395
googlers766183395
pharmgkbrs766183395
gwascentralrs766183395
openSNPrs766183395
23andMers766183395
23andMe allrs766183395
SNP Nexus

SNPshotrs766183395
SNPdbers766183395
MSV3drs766183395
GWAS Ctlgrs766183395
Max Magnitude0
ClinVar
Risk rs766183395(A;A)
Alt rs766183395(A;A)
Reference rs766183395(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121177169G>A
CLNSRC
CLNACC RCV000185704.1,