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rs118204014

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204014(C;T)
Make rs118204014(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7224966
GeneACADVL, DVL2
is asnp
is mentioned by
dbSNPrs118204014
ebirs118204014
HLIrs118204014
Exacrs118204014
Varsomers118204014
Maprs118204014
PheGenIrs118204014
hapmaprs118204014
1000 genomesrs118204014
hgdprs118204014
ensemblrs118204014
gopubmedrs118204014
geneviewrs118204014
scholarrs118204014
googlers118204014
pharmgkbrs118204014
gwascentralrs118204014
openSNPrs118204014
23andMers118204014
23andMe allrs118204014
SNP Nexus

SNPshotrs118204014
SNPdbers118204014
MSV3drs118204014
GWAS Ctlgrs118204014
Max Magnitude0
OMIM609575
Desc
Variant0003
Relatedalso
ClinVar
Risk rs118204014(T;T)
Alt rs118204014(T;T)
Reference rs118204014(C;C)
Significance Other
Disease Very long chain acyl-CoA dehydrogenase deficiency not provided
Variation info
Gene MIR324 ACADVL DVL2
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000017.10:g.7128285C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001690.5, RCV000185733.2,