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rs387906403

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906403(A;A)
Make rs387906403(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position112956192
GeneLOC100506392, SLC16A1
is asnp
is mentioned by
dbSNPrs387906403
ebirs387906403
HLIrs387906403
Exacrs387906403
Varsomers387906403
Maprs387906403
PheGenIrs387906403
hapmaprs387906403
1000 genomesrs387906403
hgdprs387906403
ensemblrs387906403
gopubmedrs387906403
geneviewrs387906403
scholarrs387906403
googlers387906403
pharmgkbrs387906403
gwascentralrs387906403
openSNPrs387906403
23andMers387906403
23andMe allrs387906403
SNP Nexus

SNPshotrs387906403
SNPdbers387906403
MSV3drs387906403
GWAS Ctlgrs387906403
Max Magnitude0
ClinVar
Risk rs387906403(A;A)
Alt rs387906403(A;A)
Reference rs387906403(G;G)
Significance Pathogenic
Disease Exercise-induced hyperinsulinemic hypoglycemia
Variation info
Gene SLC16A1 SLC16A1-AS1
CLNDBN Exercise-induced hyperinsulinemic hypoglycemia
Reversed 1
HGVS NC_000001.10:g.113498814C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009471.3,