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rs375717077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs375717077(C;T)
Make rs375717077(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position108027757
GeneHADH
is asnp
is mentioned by
dbSNPrs375717077
ebirs375717077
HLIrs375717077
Exacrs375717077
Varsomers375717077
Maprs375717077
PheGenIrs375717077
hapmaprs375717077
1000 genomesrs375717077
hgdprs375717077
ensemblrs375717077
gopubmedrs375717077
geneviewrs375717077
scholarrs375717077
googlers375717077
pharmgkbrs375717077
gwascentralrs375717077
openSNPrs375717077
23andMers375717077
23andMe allrs375717077
SNP Nexus

SNPshotrs375717077
SNPdbers375717077
MSV3drs375717077
GWAS Ctlgrs375717077
Max Magnitude0
ClinVar
Risk rs375717077(T;T)
Alt rs375717077(T;T)
Reference rs375717077(C;C)
Significance Pathogenic
Disease Hyperinsulinemic hypoglycemia
Variation info
Gene HADH
CLNDBN Hyperinsulinemic hypoglycemia, familial, 4
Reversed 0
HGVS NC_000004.11:g.108948913C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032678.2,