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rs753108198

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs753108198(-;-)
Make rs753108198(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7222675
GeneACADVL
is asnp
is mentioned by
dbSNPrs753108198
ebirs753108198
HLIrs753108198
Exacrs753108198
Varsomers753108198
Maprs753108198
PheGenIrs753108198
hapmaprs753108198
1000 genomesrs753108198
hgdprs753108198
ensemblrs753108198
gopubmedrs753108198
geneviewrs753108198
scholarrs753108198
googlers753108198
pharmgkbrs753108198
gwascentralrs753108198
openSNPrs753108198
23andMers753108198
23andMe allrs753108198
SNP Nexus

SNPshotrs753108198
SNPdbers753108198
MSV3drs753108198
GWAS Ctlgrs753108198
Max Magnitude0
ClinVar
Risk rs753108198(;)
Alt rs753108198(;)
Reference rs753108198(CT;CT)
Significance Pathogenic
Disease Very long chain acyl-CoA dehydrogenase deficiency not provided
Variation info
Gene ACADVL
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000017.10:g.7125994_7125995delCT
CLNSRC
CLNACC RCV000169392.1, RCV000185736.1,