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rs142761835

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142761835(A;A)
Make rs142761835(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position40410699
GeneIVD
is asnp
is mentioned by
dbSNPrs142761835
ebirs142761835
HLIrs142761835
Exacrs142761835
Varsomers142761835
Maprs142761835
PheGenIrs142761835
hapmaprs142761835
1000 genomesrs142761835
hgdprs142761835
ensemblrs142761835
gopubmedrs142761835
geneviewrs142761835
scholarrs142761835
googlers142761835
pharmgkbrs142761835
gwascentralrs142761835
openSNPrs142761835
23andMers142761835
23andMe allrs142761835
SNP Nexus

SNPshotrs142761835
SNPdbers142761835
MSV3drs142761835
GWAS Ctlgrs142761835
Max Magnitude0
ClinVar
Risk rs142761835(A;A)
Alt rs142761835(A;A)
Reference rs142761835(G;G)
Significance Other
Disease not provided Isovaleryl-CoA dehydrogenase deficiency
Variation info
Gene IVD
CLNDBN not provided Isovaleryl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000015.9:g.40702898G>A
CLNSRC HGMD
CLNACC RCV000153385.2, RCV000169054.2,