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rs869025177

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025177(-;-)
Make rs869025177(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71362120
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs869025177
ebirs869025177
HLIrs869025177
Exacrs869025177
Varsomers869025177
Maprs869025177
PheGenIrs869025177
hapmaprs869025177
1000 genomesrs869025177
hgdprs869025177
ensemblrs869025177
gopubmedrs869025177
geneviewrs869025177
scholarrs869025177
googlers869025177
pharmgkbrs869025177
gwascentralrs869025177
openSNPrs869025177
23andMers869025177
23andMe allrs869025177
SNP Nexus

SNPshotrs869025177
SNPdbers869025177
MSV3drs869025177
GWAS Ctlgrs869025177
Max Magnitude0
ClinVar
Risk rs869025177(;)
Alt rs869025177(;)
Reference rs869025177(T;T)
Significance Pathogenic
Disease Histiocytosis-lymphadenopathy plus syndrome
Variation info
Gene SLC29A3
CLNDBN Histiocytosis-lymphadenopathy plus syndrome
Reversed 0
HGVS NC_000010.10:g.73121877delT
CLNSRC OMIM Allelic Variant SLC29A3 @ LOVD
CLNACC RCV000000597.2,