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rs373890183

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs373890183
ClinGenrs373890183
ebirs373890183
HLIrs373890183
Exacrs373890183
Gnomadrs373890183
Varsomers373890183
LitVarrs373890183
Maprs373890183
PheGenIrs373890183
Biobankrs373890183
1000 genomesrs373890183
hgdprs373890183
ensemblrs373890183
geneviewrs373890183
scholarrs373890183
googlers373890183
pharmgkbrs373890183
gwascentralrs373890183
openSNPrs373890183
23andMers373890183
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,