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rs746408350

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746408350(C;T)
Make rs746408350(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position71322827
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs746408350
ebirs746408350
HLIrs746408350
Exacrs746408350
Varsomers746408350
Maprs746408350
PheGenIrs746408350
hapmaprs746408350
1000 genomesrs746408350
hgdprs746408350
ensemblrs746408350
gopubmedrs746408350
geneviewrs746408350
scholarrs746408350
googlers746408350
pharmgkbrs746408350
gwascentralrs746408350
openSNPrs746408350
23andMers746408350
23andMe allrs746408350
SNP Nexus

SNPshotrs746408350
SNPdbers746408350
MSV3drs746408350
GWAS Ctlgrs746408350
Max Magnitude0
ClinVar
Risk rs746408350(T;T)
Alt rs746408350(T;T)
Reference rs746408350(C;C)
Significance Pathogenic
Disease Histiocytosis-lymphadenopathy plus syndrome
Variation info
Gene SLC29A3
CLNDBN Histiocytosis-lymphadenopathy plus syndrome
Reversed 0
HGVS NC_000010.10:g.73082584C>T
CLNSRC
CLNACC RCV000192336.1,