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rs113994168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113994168(C;T)
Make rs113994168(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7222203
GeneACADVL
is asnp
is mentioned by
dbSNPrs113994168
ebirs113994168
HLIrs113994168
Exacrs113994168
Varsomers113994168
Maprs113994168
PheGenIrs113994168
hapmaprs113994168
1000 genomesrs113994168
hgdprs113994168
ensemblrs113994168
gopubmedrs113994168
geneviewrs113994168
scholarrs113994168
googlers113994168
pharmgkbrs113994168
gwascentralrs113994168
openSNPrs113994168
23andMers113994168
23andMe allrs113994168
SNP Nexus

SNPshotrs113994168
SNPdbers113994168
MSV3drs113994168
GWAS Ctlgrs113994168
Max Magnitude0
ClinVar
Risk rs113994168(T;T)
Alt rs113994168(T;T)
Reference rs113994168(C;C)
Significance Other
Disease Very long chain acyl-CoA dehydrogenase deficiency
Variation info
Gene ACADVL
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000017.10:g.7125522C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020080.3,


OMIM201475
Desc
Variant
Relatedalso