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rs797045209

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045209(C;T)
Make rs797045209(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17404525
GeneABCC8
is asnp
is mentioned by
dbSNPrs797045209
ebirs797045209
HLIrs797045209
Exacrs797045209
Varsomers797045209
Maprs797045209
PheGenIrs797045209
hapmaprs797045209
1000 genomesrs797045209
hgdprs797045209
ensemblrs797045209
gopubmedrs797045209
geneviewrs797045209
scholarrs797045209
googlers797045209
pharmgkbrs797045209
gwascentralrs797045209
openSNPrs797045209
23andMers797045209
23andMe allrs797045209
SNP Nexus

SNPshotrs797045209
SNPdbers797045209
MSV3drs797045209
GWAS Ctlgrs797045209
Max Magnitude0
ClinVar
Risk rs797045209(T;T)
Alt rs797045209(T;T)
Reference rs797045209(C;C)
Significance Pathogenic
Disease Transient neonatal diabetes mellitus 2
Variation info
Gene ABCC8
CLNDBN Transient neonatal diabetes mellitus 2
Reversed 1
HGVS NC_000011.9:g.17426072G>A
CLNSRC
CLNACC RCV000192916.1,