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rs796051910

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051910(G;G)
Make rs796051910(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7222732
GeneACADVL
is asnp
is mentioned by
dbSNPrs796051910
ClinGenrs796051910
ebirs796051910
HLIrs796051910
Exacrs796051910
Varsomers796051910
Maprs796051910
PheGenIrs796051910
hapmaprs796051910
1000 genomesrs796051910
hgdprs796051910
ensemblrs796051910
gopubmedrs796051910
geneviewrs796051910
scholarrs796051910
googlers796051910
pharmgkbrs796051910
gwascentralrs796051910
openSNPrs796051910
23andMers796051910
23andMe allrs796051910
SNP Nexus

SNPshotrs796051910
SNPdbers796051910
MSV3drs796051910
GWAS Ctlgrs796051910
Max Magnitude0
ClinVar
Risk rs796051910(G;G)
Alt rs796051910(G;G)
Reference Rs796051910(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7126051T>G
CLNSRC
CLNACC RCV000185716.1,