Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783674

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783674(C;G)
Make rs587783674(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17388084
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs587783674
ebirs587783674
HLIrs587783674
Exacrs587783674
Varsomers587783674
Maprs587783674
PheGenIrs587783674
hapmaprs587783674
1000 genomesrs587783674
hgdprs587783674
ensemblrs587783674
gopubmedrs587783674
geneviewrs587783674
scholarrs587783674
googlers587783674
pharmgkbrs587783674
gwascentralrs587783674
openSNPrs587783674
23andMers587783674
23andMe allrs587783674
SNP Nexus

SNPshotrs587783674
SNPdbers587783674
MSV3drs587783674
GWAS Ctlgrs587783674
Max Magnitude0
ClinVar
Risk rs587783674(G;G)
Alt rs587783674(G;G)
Reference rs587783674(C;C)
Significance Pathogenic
Disease Neonatal insulin-dependent diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Neonatal insulin-dependent diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17409631G>C
CLNSRC
CLNACC RCV000146121.1,