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rs141957107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141957107(C;T)
Make rs141957107(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position227688165
GeneSLC19A3
is asnp
is mentioned by
dbSNPrs141957107
dbSNP (old)rs141957107
ClinGenrs141957107
ebirs141957107
HLIrs141957107
Exacrs141957107
Gnomadrs141957107
Varsomers141957107
LitVarrs141957107
Maprs141957107
PheGenIrs141957107
Biobankrs141957107
1000 genomesrs141957107
hgdprs141957107
ensemblrs141957107
gopubmedrs141957107
geneviewrs141957107
scholarrs141957107
googlers141957107
pharmgkbrs141957107
gwascentralrs141957107
openSNPrs141957107
23andMers141957107
23andMe allrs141957107
SNPshotrs141957107
SNPdbers141957107
MSV3drs141957107
GWAS Ctlgrs141957107
Max Magnitude0
ClinVar
Risk rs141957107(T;T)
Alt rs141957107(T;T)
Reference Rs141957107(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC19A3
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.228552881C>T
CLNSRC
CLNACC RCV000255502.1,