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rs373890183

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373890183(A;A)
Make rs373890183(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position21848201
GeneABCC9
is asnp
is mentioned by
dbSNPrs373890183
ebirs373890183
HLIrs373890183
Exacrs373890183
Varsomers373890183
Maprs373890183
PheGenIrs373890183
hapmaprs373890183
1000 genomesrs373890183
hgdprs373890183
ensemblrs373890183
gopubmedrs373890183
geneviewrs373890183
scholarrs373890183
googlers373890183
pharmgkbrs373890183
gwascentralrs373890183
openSNPrs373890183
23andMers373890183
23andMe allrs373890183
SNP Nexus

SNPshotrs373890183
SNPdbers373890183
MSV3drs373890183
GWAS Ctlgrs373890183
Max Magnitude0
ClinVar
Risk rs373890183(A;A)
Alt rs373890183(A;A)
Reference rs373890183(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.22001135G>A
CLNSRC
CLNACC RCV000171208.1,