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rs796051906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGC;CGC) 0 common in clinvar
Make rs796051906(CGC;TGT)
Make rs796051906(TGT;TGT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120738874
GeneACADS
is asnp
is mentioned by
dbSNPrs796051906
ClinGenrs796051906
ebirs796051906
HLIrs796051906
Exacrs796051906
Varsomers796051906
Maprs796051906
PheGenIrs796051906
hapmaprs796051906
1000 genomesrs796051906
hgdprs796051906
ensemblrs796051906
gopubmedrs796051906
geneviewrs796051906
scholarrs796051906
googlers796051906
pharmgkbrs796051906
gwascentralrs796051906
openSNPrs796051906
23andMers796051906
23andMe allrs796051906
SNP Nexus

SNPshotrs796051906
SNPdbers796051906
MSV3drs796051906
GWAS Ctlgrs796051906
Max Magnitude0
ClinVar
Risk rs796051906(TGT;TGT)
Alt rs796051906(TGT;TGT)
Reference Rs796051906(CGC;CGC)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121176677_121176679delCGCinsTGT
CLNSRC
CLNACC RCV000185708.3,