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rs797045637

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045637(C;C)
Make rs797045637(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17387226
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs797045637
ebirs797045637
HLIrs797045637
Exacrs797045637
Varsomers797045637
Maprs797045637
PheGenIrs797045637
hapmaprs797045637
1000 genomesrs797045637
hgdprs797045637
ensemblrs797045637
gopubmedrs797045637
geneviewrs797045637
scholarrs797045637
googlers797045637
pharmgkbrs797045637
gwascentralrs797045637
openSNPrs797045637
23andMers797045637
23andMe allrs797045637
SNP Nexus

SNPshotrs797045637
SNPdbers797045637
MSV3drs797045637
GWAS Ctlgrs797045637
Max Magnitude0
ClinVar
Risk rs797045637(C,T;C,T)
Alt rs797045637(C,T;C,T)
Reference rs797045637(G;G)
Significance Probable-Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 1
HGVS NC_000011.9:g.17408773C>A; NC_000011.9:g.17408773C>G
CLNSRC
CLNACC RCV000194466.1, RCV000193250.1,