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rs587783673

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783673(A;A)
Make rs587783673(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17387407
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs587783673
ebirs587783673
HLIrs587783673
Exacrs587783673
Varsomers587783673
Maprs587783673
PheGenIrs587783673
hapmaprs587783673
1000 genomesrs587783673
hgdprs587783673
ensemblrs587783673
gopubmedrs587783673
geneviewrs587783673
scholarrs587783673
googlers587783673
pharmgkbrs587783673
gwascentralrs587783673
openSNPrs587783673
23andMers587783673
23andMe allrs587783673
SNP Nexus

SNPshotrs587783673
SNPdbers587783673
MSV3drs587783673
GWAS Ctlgrs587783673
Max Magnitude0
ClinVar
Risk rs587783673(A;A)
Alt rs587783673(A;A)
Reference rs587783673(G;G)
Significance Pathogenic
Disease Diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17408954C>T
CLNSRC
CLNACC RCV000146117.1,