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rs397517184

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517184(C;C)
Make rs397517184(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position21906141
GeneABCC9
is asnp
is mentioned by
dbSNPrs397517184
ebirs397517184
HLIrs397517184
Exacrs397517184
Varsomers397517184
Maprs397517184
PheGenIrs397517184
hapmaprs397517184
1000 genomesrs397517184
hgdprs397517184
ensemblrs397517184
gopubmedrs397517184
geneviewrs397517184
scholarrs397517184
googlers397517184
pharmgkbrs397517184
gwascentralrs397517184
openSNPrs397517184
23andMers397517184
23andMe allrs397517184
SNP Nexus

SNPshotrs397517184
SNPdbers397517184
MSV3drs397517184
GWAS Ctlgrs397517184
Max Magnitude0
ClinVar
Risk rs397517184(C;C)
Alt rs397517184(C;C)
Reference rs397517184(T;T)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene ABCC9
CLNDBN not specified not provided
Reversed 1
HGVS NC_000012.11:g.22059075A>G
CLNSRC
CLNACC RCV000038586.2, RCV000171210.1,