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

rs786204613

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204613(-;-)
Make rs786204613(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40418170
GeneIVD
is asnp
is mentioned by
dbSNPrs786204613
ebirs786204613
HLIrs786204613
Exacrs786204613
Varsomers786204613
Maprs786204613
PheGenIrs786204613
hapmaprs786204613
1000 genomesrs786204613
hgdprs786204613
ensemblrs786204613
gopubmedrs786204613
geneviewrs786204613
scholarrs786204613
googlers786204613
pharmgkbrs786204613
gwascentralrs786204613
openSNPrs786204613
23andMers786204613
23andMe allrs786204613
SNP Nexus

SNPshotrs786204613
SNPdbers786204613
MSV3drs786204613
GWAS Ctlgrs786204613
Max Magnitude0
ClinVar
Risk rs786204613(;)
Alt rs786204613(;)
Reference rs786204613(T;T)
Significance Probable-Pathogenic
Disease Isovaleryl-CoA dehydrogenase deficiency
Variation info
Gene IVD
CLNDBN Isovaleryl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000015.9:g.40710369delT
CLNSRC
CLNACC RCV000169373.1,