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rs786204738

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204738(C;T)
Make rs786204738(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7221014
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs786204738
ebirs786204738
HLIrs786204738
Exacrs786204738
Varsomers786204738
Maprs786204738
PheGenIrs786204738
hapmaprs786204738
1000 genomesrs786204738
hgdprs786204738
ensemblrs786204738
gopubmedrs786204738
geneviewrs786204738
scholarrs786204738
googlers786204738
pharmgkbrs786204738
gwascentralrs786204738
openSNPrs786204738
23andMers786204738
23andMe allrs786204738
SNP Nexus

SNPshotrs786204738
SNPdbers786204738
MSV3drs786204738
GWAS Ctlgrs786204738
Max Magnitude0
ClinVar
Risk rs786204738(T;T)
Alt rs786204738(T;T)
Reference rs786204738(C;C)
Significance Probable-Pathogenic
Disease Very long chain acyl-CoA dehydrogenase deficiency
Variation info
Gene DLG4 ACADVL
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000017.10:g.7124333C>T
CLNSRC
CLNACC RCV000169585.1,