Have questions? Visit https://www.reddit.com/r/SNPedia

rs763130915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACG;ACG) 0 common in clinvar
Make rs763130915(-;-)
Make rs763130915(-;ACG)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position227699210
GeneSLC19A3
is asnp
is mentioned by
dbSNPrs763130915
dbSNP (classic)rs763130915
ClinGenrs763130915
ebirs763130915
HLIrs763130915
Exacrs763130915
Gnomadrs763130915
Varsomers763130915
LitVarrs763130915
Maprs763130915
PheGenIrs763130915
Biobankrs763130915
1000 genomesrs763130915
hgdprs763130915
ensemblrs763130915
geneviewrs763130915
scholarrs763130915
googlers763130915
pharmgkbrs763130915
gwascentralrs763130915
openSNPrs763130915
23andMers763130915
SNPshotrs763130915
SNPdbers763130915
MSV3drs763130915
GWAS Ctlgrs763130915
Max Magnitude0
ClinVar
Risk rs763130915(-;-)
Alt rs763130915(-;-)
Reference Rs763130915(ACG;ACG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC19A3
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.228563926_228563928delACG
CLNSRC
CLNACC RCV000486999.1,