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rs267607196

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607196(A;A)
Make rs267607196(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position17387248
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs267607196
ebirs267607196
HLIrs267607196
Exacrs267607196
Varsomers267607196
Maprs267607196
PheGenIrs267607196
hapmaprs267607196
1000 genomesrs267607196
hgdprs267607196
ensemblrs267607196
gopubmedrs267607196
geneviewrs267607196
scholarrs267607196
googlers267607196
pharmgkbrs267607196
gwascentralrs267607196
openSNPrs267607196
23andMers267607196
23andMe allrs267607196
SNP Nexus

SNPshotrs267607196
SNPdbers267607196
MSV3drs267607196
GWAS Ctlgrs267607196
Max Magnitude0
ClinVar
Risk rs267607196(A;A)
Alt rs267607196(A;A)
Reference rs267607196(G;G)
Significance Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 1
HGVS NC_000011.9:g.17408795C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009223.5,