Have questions? Visit https://www.reddit.com/r/SNPedia

rs369560930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369560930(A;A)
Make rs369560930(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7221580
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs369560930
ebirs369560930
HLIrs369560930
Exacrs369560930
Varsomers369560930
Maprs369560930
PheGenIrs369560930
hapmaprs369560930
1000 genomesrs369560930
hgdprs369560930
ensemblrs369560930
gopubmedrs369560930
geneviewrs369560930
scholarrs369560930
googlers369560930
pharmgkbrs369560930
gwascentralrs369560930
openSNPrs369560930
23andMers369560930
23andMe allrs369560930
SNP Nexus

SNPshotrs369560930
SNPdbers369560930
MSV3drs369560930
GWAS Ctlgrs369560930
Max Magnitude0
ClinVar
Risk rs369560930(A,T;A,T)
Alt rs369560930(A,T;A,T)
Reference rs369560930(G;G)
Significance Pathogenic
Disease not provided Very long chain acyl-CoA dehydrogenase deficiency
Variation info
Gene DLG4 ACADVL
CLNDBN not provided Very long chain acyl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000017.10:g.7124899G>A
CLNSRC HGMD
CLNACC RCV000077919.3, RCV000179696.1,