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rs80356635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs80356635(C;C)
Make rs80356635(C;T)
ReferenceGRCh37 37.1/132
Chromosome11
Position17496466
GeneABCC8
is asnp
is mentioned by
dbSNPrs80356635
ebirs80356635
HLIrs80356635
Exacrs80356635
Varsomers80356635
Maprs80356635
PheGenIrs80356635
hapmaprs80356635
1000 genomesrs80356635
hgdprs80356635
ensemblrs80356635
gopubmedrs80356635
geneviewrs80356635
scholarrs80356635
googlers80356635
pharmgkbrs80356635
gwascentralrs80356635
openSNPrs80356635
23andMers80356635
23andMe allrs80356635
SNP Nexus

SNPshotrs80356635
SNPdbers80356635
MSV3drs80356635
GWAS Ctlgrs80356635
StatusDeleted
Max Magnitude0
OMIM600509
Desc
Variant0026
Relatedalso
[PMID 17668386OA-icon.png] Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.