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rs755856935

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs755856935(A;G)
Make rs755856935(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120737845
GeneACADS
is asnp
is mentioned by
dbSNPrs755856935
ebirs755856935
HLIrs755856935
Exacrs755856935
Varsomers755856935
Maprs755856935
PheGenIrs755856935
hapmaprs755856935
1000 genomesrs755856935
hgdprs755856935
ensemblrs755856935
gopubmedrs755856935
geneviewrs755856935
scholarrs755856935
googlers755856935
pharmgkbrs755856935
gwascentralrs755856935
openSNPrs755856935
23andMers755856935
23andMe allrs755856935
SNP Nexus

SNPshotrs755856935
SNPdbers755856935
MSV3drs755856935
GWAS Ctlgrs755856935
Max Magnitude0
ClinVar
Risk rs755856935(G;G)
Alt rs755856935(G;G)
Reference rs755856935(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121175648A>G
CLNSRC
CLNACC RCV000185682.1,