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rs587783171

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783171(G;G)
Make rs587783171(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17395876
GeneABCC8
is asnp
is mentioned by
dbSNPrs587783171
ebirs587783171
HLIrs587783171
Exacrs587783171
Varsomers587783171
Maprs587783171
PheGenIrs587783171
hapmaprs587783171
1000 genomesrs587783171
hgdprs587783171
ensemblrs587783171
gopubmedrs587783171
geneviewrs587783171
scholarrs587783171
googlers587783171
pharmgkbrs587783171
gwascentralrs587783171
openSNPrs587783171
23andMers587783171
23andMe allrs587783171
SNP Nexus

SNPshotrs587783171
SNPdbers587783171
MSV3drs587783171
GWAS Ctlgrs587783171
Max Magnitude0
ClinVar
Risk rs587783171(G;G)
Alt rs587783171(G;G)
Reference rs587783171(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCC8
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.17417423A>C
CLNSRC
CLNACC RCV000144999.1,