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rs74339576

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0 common in clinvar
Make rs74339576(A;A)
Make rs74339576(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position17387190
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs74339576
ebirs74339576
HLIrs74339576
Exacrs74339576
Varsomers74339576
Maprs74339576
PheGenIrs74339576
hapmaprs74339576
1000 genomesrs74339576
hgdprs74339576
ensemblrs74339576
gopubmedrs74339576
geneviewrs74339576
scholarrs74339576
googlers74339576
pharmgkbrs74339576
gwascentralrs74339576
openSNPrs74339576
23andMers74339576
23andMe allrs74339576
SNP Nexus

SNPshotrs74339576
SNPdbers74339576
MSV3drs74339576
GWAS Ctlgrs74339576
GMAF0.0004591
Max Magnitude0
OMIM600937
Desc
Variant0019
Relatedalso
ClinVar
Risk rs74339576(A,T;A,T)
Alt rs74339576(A,T;A,T)
Reference rs74339576(G;G)
Significance Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 1
HGVS NC_000011.9:g.17408737C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009220.2,