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rs771075821

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771075821(A;A)
Make rs771075821(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17476705
GeneABCC8
is asnp
is mentioned by
dbSNPrs771075821
ebirs771075821
HLIrs771075821
Exacrs771075821
Varsomers771075821
Maprs771075821
PheGenIrs771075821
hapmaprs771075821
1000 genomesrs771075821
hgdprs771075821
ensemblrs771075821
gopubmedrs771075821
geneviewrs771075821
scholarrs771075821
googlers771075821
pharmgkbrs771075821
gwascentralrs771075821
openSNPrs771075821
23andMers771075821
23andMe allrs771075821
SNP Nexus

SNPshotrs771075821
SNPdbers771075821
MSV3drs771075821
GWAS Ctlgrs771075821
Max Magnitude0
ClinVar
Risk rs771075821(A;A)
Alt rs771075821(A;A)
Reference rs771075821(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCC8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.17498252G>T
CLNSRC
CLNACC RCV000201893.1,