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rs587780462

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780462(C;T)
Make rs587780462(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position71362408
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs587780462
ebirs587780462
HLIrs587780462
Exacrs587780462
Varsomers587780462
Maprs587780462
PheGenIrs587780462
hapmaprs587780462
1000 genomesrs587780462
hgdprs587780462
ensemblrs587780462
gopubmedrs587780462
geneviewrs587780462
scholarrs587780462
googlers587780462
pharmgkbrs587780462
gwascentralrs587780462
openSNPrs587780462
23andMers587780462
23andMe allrs587780462
SNP Nexus

SNPshotrs587780462
SNPdbers587780462
MSV3drs587780462
GWAS Ctlgrs587780462
Max Magnitude0
ClinVar
Risk rs587780462(T;T)
Alt rs587780462(T;T)
Reference rs587780462(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.73122165C>T
CLNSRC
CLNACC RCV000118376.1,