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rs786204607

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204607(C;T)
Make rs786204607(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26215149
GeneHADHA
is asnp
is mentioned by
dbSNPrs786204607
ebirs786204607
HLIrs786204607
Exacrs786204607
Varsomers786204607
Maprs786204607
PheGenIrs786204607
hapmaprs786204607
1000 genomesrs786204607
hgdprs786204607
ensemblrs786204607
gopubmedrs786204607
geneviewrs786204607
scholarrs786204607
googlers786204607
pharmgkbrs786204607
gwascentralrs786204607
openSNPrs786204607
23andMers786204607
23andMe allrs786204607
SNP Nexus

SNPshotrs786204607
SNPdbers786204607
MSV3drs786204607
GWAS Ctlgrs786204607
Max Magnitude0
ClinVar
Risk rs786204607(T;T)
Alt rs786204607(T;T)
Reference rs786204607(C;C)
Significance Probable-Pathogenic
Disease Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Variation info
Gene HADHA
CLNDBN Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Reversed 1
HGVS NC_000002.11:g.26438018G>A
CLNSRC
CLNACC RCV000169366.1,