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rs368469075

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368469075(G;T)
Make rs368469075(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120739304
GeneACADS
is asnp
is mentioned by
dbSNPrs368469075
ebirs368469075
HLIrs368469075
Exacrs368469075
Varsomers368469075
Maprs368469075
PheGenIrs368469075
hapmaprs368469075
1000 genomesrs368469075
hgdprs368469075
ensemblrs368469075
gopubmedrs368469075
geneviewrs368469075
scholarrs368469075
googlers368469075
pharmgkbrs368469075
gwascentralrs368469075
openSNPrs368469075
23andMers368469075
23andMe allrs368469075
SNP Nexus

SNPshotrs368469075
SNPdbers368469075
MSV3drs368469075
GWAS Ctlgrs368469075
Max Magnitude0
ClinVar
Risk rs368469075(T;T)
Alt rs368469075(T;T)
Reference rs368469075(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121177107G>T
CLNSRC
CLNACC RCV000185694.2,