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rs869025176

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025176(-;-)
Make rs869025176(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71362225
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs869025176
ebirs869025176
HLIrs869025176
Exacrs869025176
Varsomers869025176
Maprs869025176
PheGenIrs869025176
hapmaprs869025176
1000 genomesrs869025176
hgdprs869025176
ensemblrs869025176
gopubmedrs869025176
geneviewrs869025176
scholarrs869025176
googlers869025176
pharmgkbrs869025176
gwascentralrs869025176
openSNPrs869025176
23andMers869025176
23andMe allrs869025176
SNP Nexus

SNPshotrs869025176
SNPdbers869025176
MSV3drs869025176
GWAS Ctlgrs869025176
Max Magnitude0
ClinVar
Risk rs869025176(;)
Alt rs869025176(;)
Reference rs869025176(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.73121982delC
CLNSRC OMIM Allelic Variant SLC29A3 @ LOVD
CLNACC RCV000000596.2,