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rs752507753

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752507753(A;A)
Make rs752507753(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17388013
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs752507753
ebirs752507753
HLIrs752507753
Exacrs752507753
Varsomers752507753
Maprs752507753
PheGenIrs752507753
hapmaprs752507753
1000 genomesrs752507753
hgdprs752507753
ensemblrs752507753
gopubmedrs752507753
geneviewrs752507753
scholarrs752507753
googlers752507753
pharmgkbrs752507753
gwascentralrs752507753
openSNPrs752507753
23andMers752507753
23andMe allrs752507753
SNP Nexus

SNPshotrs752507753
SNPdbers752507753
MSV3drs752507753
GWAS Ctlgrs752507753
Max Magnitude0
ClinVar
Risk rs752507753(A;A)
Alt rs752507753(A;A)
Reference rs752507753(G;G)
Significance Probable-Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 0
HGVS NC_000011.9:g.17409560G>A
CLNSRC
CLNACC RCV000193401.1,