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rs863224205

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224205(C;G)
Make rs863224205(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position227687410
GeneSLC19A3
is asnp
is mentioned by
dbSNPrs863224205
ebirs863224205
HLIrs863224205
Exacrs863224205
Varsomers863224205
Maprs863224205
PheGenIrs863224205
hapmaprs863224205
1000 genomesrs863224205
hgdprs863224205
ensemblrs863224205
gopubmedrs863224205
geneviewrs863224205
scholarrs863224205
googlers863224205
pharmgkbrs863224205
gwascentralrs863224205
openSNPrs863224205
23andMers863224205
23andMe allrs863224205
SNP Nexus

SNPshotrs863224205
SNPdbers863224205
MSV3drs863224205
GWAS Ctlgrs863224205
Max Magnitude0
ClinVar
Risk rs863224205(G;G)
Alt rs863224205(G;G)
Reference rs863224205(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC19A3
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.228552126G>C
CLNSRC
CLNACC RCV000199348.1,