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rs141322087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141322087(C;T)
Make rs141322087(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17404552
GeneABCC8
is asnp
is mentioned by
dbSNPrs141322087
ebirs141322087
HLIrs141322087
Exacrs141322087
Varsomers141322087
Maprs141322087
PheGenIrs141322087
hapmaprs141322087
1000 genomesrs141322087
hgdprs141322087
ensemblrs141322087
gopubmedrs141322087
geneviewrs141322087
scholarrs141322087
googlers141322087
pharmgkbrs141322087
gwascentralrs141322087
openSNPrs141322087
23andMers141322087
23andMe allrs141322087
SNP Nexus

SNPshotrs141322087
SNPdbers141322087
MSV3drs141322087
GWAS Ctlgrs141322087
Max Magnitude0
ClinVar
Risk rs141322087(T;T)
Alt rs141322087(T;T)
Reference rs141322087(C;C)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene ABCC8
CLNDBN Neonatal diabetes mellitus
Reversed 0
HGVS NC_000011.9:g.17426099C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029255.1,