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rs780957825

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs780957825(A;A)
Make rs780957825(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17387211
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs780957825
ebirs780957825
HLIrs780957825
Exacrs780957825
Varsomers780957825
Maprs780957825
PheGenIrs780957825
hapmaprs780957825
1000 genomesrs780957825
hgdprs780957825
ensemblrs780957825
gopubmedrs780957825
geneviewrs780957825
scholarrs780957825
googlers780957825
pharmgkbrs780957825
gwascentralrs780957825
openSNPrs780957825
23andMers780957825
23andMe allrs780957825
SNP Nexus

SNPshotrs780957825
SNPdbers780957825
MSV3drs780957825
GWAS Ctlgrs780957825
Max Magnitude0
ClinVar
Risk rs780957825(A;A)
Alt rs780957825(A;A)
Reference rs780957825(G;G)
Significance Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 0
HGVS NC_000011.9:g.17408758G>A
CLNSRC
CLNACC RCV000192330.1,