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rs587783671

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783671(A;C)
Make rs587783671(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17387556
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs587783671
ebirs587783671
HLIrs587783671
Exacrs587783671
Varsomers587783671
Maprs587783671
PheGenIrs587783671
hapmaprs587783671
1000 genomesrs587783671
hgdprs587783671
ensemblrs587783671
gopubmedrs587783671
geneviewrs587783671
scholarrs587783671
googlers587783671
pharmgkbrs587783671
gwascentralrs587783671
openSNPrs587783671
23andMers587783671
23andMe allrs587783671
SNP Nexus

SNPshotrs587783671
SNPdbers587783671
MSV3drs587783671
GWAS Ctlgrs587783671
Max Magnitude0
ClinVar
Risk rs587783671(C;C)
Alt rs587783671(C;C)
Reference rs587783671(A;A)
Significance Probable-Pathogenic
Disease Neonatal insulin-dependent diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Neonatal insulin-dependent diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17409103T>G
CLNSRC
CLNACC RCV000146109.1,