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rs760889253

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760889253(A;A)
Make rs760889253(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position21882807
GeneABCC9
is asnp
is mentioned by
dbSNPrs760889253
ebirs760889253
HLIrs760889253
Exacrs760889253
Varsomers760889253
Maprs760889253
PheGenIrs760889253
hapmaprs760889253
1000 genomesrs760889253
hgdprs760889253
ensemblrs760889253
gopubmedrs760889253
geneviewrs760889253
scholarrs760889253
googlers760889253
pharmgkbrs760889253
gwascentralrs760889253
openSNPrs760889253
23andMers760889253
23andMe allrs760889253
SNP Nexus

SNPshotrs760889253
SNPdbers760889253
MSV3drs760889253
GWAS Ctlgrs760889253
Max Magnitude0
ClinVar
Risk rs760889253(A;A)
Alt rs760889253(A;A)
Reference rs760889253(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.22035741G>A
CLNSRC
CLNACC RCV000171209.1,