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rs786205475

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205475(C;T)
Make rs786205475(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position21838124
GeneABCC9
is asnp
is mentioned by
dbSNPrs786205475
ebirs786205475
HLIrs786205475
Exacrs786205475
Varsomers786205475
Maprs786205475
PheGenIrs786205475
hapmaprs786205475
1000 genomesrs786205475
hgdprs786205475
ensemblrs786205475
gopubmedrs786205475
geneviewrs786205475
scholarrs786205475
googlers786205475
pharmgkbrs786205475
gwascentralrs786205475
openSNPrs786205475
23andMers786205475
23andMe allrs786205475
SNP Nexus

SNPshotrs786205475
SNPdbers786205475
MSV3drs786205475
GWAS Ctlgrs786205475
Max Magnitude0
ClinVar
Risk rs786205475(T;T)
Alt rs786205475(T;T)
Reference rs786205475(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.21991058G>A
CLNSRC
CLNACC RCV000171207.1,