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

rs148529020

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148529020(C;T)
Make rs148529020(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17460613
GeneABCC8
is asnp
is mentioned by
dbSNPrs148529020
ebirs148529020
HLIrs148529020
Exacrs148529020
Varsomers148529020
Maprs148529020
PheGenIrs148529020
hapmaprs148529020
1000 genomesrs148529020
hgdprs148529020
ensemblrs148529020
gopubmedrs148529020
geneviewrs148529020
scholarrs148529020
googlers148529020
pharmgkbrs148529020
gwascentralrs148529020
openSNPrs148529020
23andMers148529020
23andMe allrs148529020
SNP Nexus

SNPshotrs148529020
SNPdbers148529020
MSV3drs148529020
GWAS Ctlgrs148529020
Max Magnitude0
ClinVar
Risk rs148529020(T;T)
Alt rs148529020(T;T)
Reference rs148529020(C;C)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene ABCC8
CLNDBN Neonatal diabetes mellitus
Reversed 0
HGVS NC_000011.9:g.17482160C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029271.1,