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rs104894237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894237(C;T)
Make rs104894237(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17387331
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs104894237
ebirs104894237
HLIrs104894237
Exacrs104894237
Varsomers104894237
Maprs104894237
PheGenIrs104894237
hapmaprs104894237
1000 genomesrs104894237
hgdprs104894237
ensemblrs104894237
gopubmedrs104894237
geneviewrs104894237
scholarrs104894237
googlers104894237
pharmgkbrs104894237
gwascentralrs104894237
openSNPrs104894237
23andMers104894237
23andMe allrs104894237
SNP Nexus

SNPshotrs104894237
SNPdbers104894237
MSV3drs104894237
GWAS Ctlgrs104894237
Max Magnitude0
OMIM600937
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104894237(T;T)
Alt rs104894237(T;T)
Reference rs104894237(C;C)
Significance Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 1
HGVS NC_000011.9:g.17408878G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009210.3,