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rs387906250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906250(-;-)
Make rs387906250(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7220923
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs387906250
ebirs387906250
HLIrs387906250
Exacrs387906250
Varsomers387906250
Maprs387906250
PheGenIrs387906250
hapmaprs387906250
1000 genomesrs387906250
hgdprs387906250
ensemblrs387906250
gopubmedrs387906250
geneviewrs387906250
scholarrs387906250
googlers387906250
pharmgkbrs387906250
gwascentralrs387906250
openSNPrs387906250
23andMers387906250
23andMe allrs387906250
SNP Nexus

SNPshotrs387906250
SNPdbers387906250
MSV3drs387906250
GWAS Ctlgrs387906250
Max Magnitude0
ClinVar
Risk rs387906250(;)
Alt rs387906250(;)
Reference rs387906250(G;G)
Significance Other
Disease Very long chain acyl-CoA dehydrogenase deficiency not provided
Variation info
Gene DLG4 ACADVL
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000017.10:g.7124243delG
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000001691.6, RCV000077915.3,