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rs786200932

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786200932(G;T)
Make rs786200932(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position108024034
GeneHADH
is asnp
is mentioned by
dbSNPrs786200932
ebirs786200932
HLIrs786200932
Exacrs786200932
Varsomers786200932
Maprs786200932
PheGenIrs786200932
hapmaprs786200932
1000 genomesrs786200932
hgdprs786200932
ensemblrs786200932
gopubmedrs786200932
geneviewrs786200932
scholarrs786200932
googlers786200932
pharmgkbrs786200932
gwascentralrs786200932
openSNPrs786200932
23andMers786200932
23andMe allrs786200932
SNP Nexus

SNPshotrs786200932
SNPdbers786200932
MSV3drs786200932
GWAS Ctlgrs786200932
Max Magnitude0
ClinVar
Risk rs786200932(T;T)
Alt rs786200932(T;T)
Reference rs786200932(G;G)
Significance Pathogenic
Disease Hyperinsulinemic hypoglycemia
Variation info
Gene HADH
CLNDBN Hyperinsulinemic hypoglycemia, familial, 4
Reversed 0
HGVS NC_000004.11:g.108945190G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032680.5,