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rs104894236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894236(A;A)
Make rs104894236(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position17388056
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs104894236
ebirs104894236
HLIrs104894236
Exacrs104894236
Varsomers104894236
Maprs104894236
PheGenIrs104894236
hapmaprs104894236
1000 genomesrs104894236
hgdprs104894236
ensemblrs104894236
gopubmedrs104894236
geneviewrs104894236
scholarrs104894236
googlers104894236
pharmgkbrs104894236
gwascentralrs104894236
openSNPrs104894236
23andMers104894236
23andMe allrs104894236
SNP Nexus

SNPshotrs104894236
SNPdbers104894236
MSV3drs104894236
GWAS Ctlgrs104894236
Max Magnitude0
OMIM600937
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104894236(A,T;A,T)
Alt rs104894236(A,T;A,T)
Reference rs104894236(C;C)
Significance Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 1
HGVS NC_000011.9:g.17409603G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009208.3,