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rs863224204

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224204(C;G)
Make rs863224204(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position227687556
GeneSLC19A3
is asnp
is mentioned by
dbSNPrs863224204
ebirs863224204
HLIrs863224204
Exacrs863224204
Varsomers863224204
Maprs863224204
PheGenIrs863224204
hapmaprs863224204
1000 genomesrs863224204
hgdprs863224204
ensemblrs863224204
gopubmedrs863224204
geneviewrs863224204
scholarrs863224204
googlers863224204
pharmgkbrs863224204
gwascentralrs863224204
openSNPrs863224204
23andMers863224204
23andMe allrs863224204
SNP Nexus

SNPshotrs863224204
SNPdbers863224204
MSV3drs863224204
GWAS Ctlgrs863224204
Max Magnitude0
ClinVar
Risk rs863224204(G;G)
Alt rs863224204(G;G)
Reference rs863224204(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC19A3
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.228552272G>C
CLNSRC
CLNACC RCV000197098.2,