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rs202124189

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202124189(G;T)
Make rs202124189(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120739362
GeneACADS
is asnp
is mentioned by
dbSNPrs202124189
ebirs202124189
HLIrs202124189
Exacrs202124189
Varsomers202124189
Maprs202124189
PheGenIrs202124189
hapmaprs202124189
1000 genomesrs202124189
hgdprs202124189
ensemblrs202124189
gopubmedrs202124189
geneviewrs202124189
scholarrs202124189
googlers202124189
pharmgkbrs202124189
gwascentralrs202124189
openSNPrs202124189
23andMers202124189
23andMe allrs202124189
SNP Nexus

SNPshotrs202124189
SNPdbers202124189
MSV3drs202124189
GWAS Ctlgrs202124189
Max Magnitude0
ClinVar
Risk rs202124189(T;T)
Alt rs202124189(T;T)
Reference rs202124189(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121177165G>A
CLNSRC
CLNACC RCV000185701.1,