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rs139964066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139964066(A;A)
Make rs139964066(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position17402671
GeneABCC8
is asnp
is mentioned by
dbSNPrs139964066
ClinGenrs139964066
ebirs139964066
HLIrs139964066
Exacrs139964066
Varsomers139964066
Maprs139964066
PheGenIrs139964066
hapmaprs139964066
1000 genomesrs139964066
hgdprs139964066
ensemblrs139964066
gopubmedrs139964066
geneviewrs139964066
scholarrs139964066
googlers139964066
pharmgkbrs139964066
gwascentralrs139964066
openSNPrs139964066
23andMers139964066
23andMe allrs139964066
SNP Nexus

SNPshotrs139964066
SNPdbers139964066
MSV3drs139964066
GWAS Ctlgrs139964066
Max Magnitude0
ClinVar
Risk rs139964066(A;A)
Alt rs139964066(A;A)
Reference Rs139964066(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCC8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.17424218G>A
CLNSRC
CLNACC RCV000223959.1,