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rs80356652

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs80356652(A;A)
Make rs80356652(A;C)
ReferenceGRCh37 37.1/132
Chromosome11
Position17426062
GeneABCC8
is asnp
is mentioned by
dbSNPrs80356652
ebirs80356652
HLIrs80356652
Exacrs80356652
Varsomers80356652
Maprs80356652
PheGenIrs80356652
hapmaprs80356652
1000 genomesrs80356652
hgdprs80356652
ensemblrs80356652
gopubmedrs80356652
geneviewrs80356652
scholarrs80356652
googlers80356652
pharmgkbrs80356652
gwascentralrs80356652
openSNPrs80356652
23andMers80356652
23andMe allrs80356652
SNP Nexus

SNPshotrs80356652
SNPdbers80356652
MSV3drs80356652
GWAS Ctlgrs80356652
StatusDeleted
Max Magnitude0
OMIM600509
Desc
Variant0023
Relatedalso
[PMID 17668386OA-icon.png] Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.