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rs863225278

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225278(A;T)
Make rs863225278(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17408519
GeneABCC8
is asnp
is mentioned by
dbSNPrs863225278
ebirs863225278
HLIrs863225278
Exacrs863225278
Varsomers863225278
Maprs863225278
PheGenIrs863225278
hapmaprs863225278
1000 genomesrs863225278
hgdprs863225278
ensemblrs863225278
gopubmedrs863225278
geneviewrs863225278
scholarrs863225278
googlers863225278
pharmgkbrs863225278
gwascentralrs863225278
openSNPrs863225278
23andMers863225278
23andMe allrs863225278
SNP Nexus

SNPshotrs863225278
SNPdbers863225278
MSV3drs863225278
GWAS Ctlgrs863225278
Max Magnitude0
ClinVar
Risk rs863225278(T;T)
Alt rs863225278(T;T)
Reference rs863225278(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCC8
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.17430066T>A
CLNSRC
CLNACC RCV000201888.1,