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rs397515429

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515429(A;A)
Make rs397515429(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71362337
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs397515429
ebirs397515429
HLIrs397515429
Exacrs397515429
Varsomers397515429
Maprs397515429
PheGenIrs397515429
hapmaprs397515429
1000 genomesrs397515429
hgdprs397515429
ensemblrs397515429
gopubmedrs397515429
geneviewrs397515429
scholarrs397515429
googlers397515429
pharmgkbrs397515429
gwascentralrs397515429
openSNPrs397515429
23andMers397515429
23andMe allrs397515429
SNP Nexus

SNPshotrs397515429
SNPdbers397515429
MSV3drs397515429
GWAS Ctlgrs397515429
Max Magnitude0
ClinVar
Risk rs397515429(A;A)
Alt rs397515429(A;A)
Reference rs397515429(G;G)
Significance Pathogenic
Disease Histiocytosis-lymphadenopathy plus syndrome
Variation info
Gene SLC29A3
CLNDBN Histiocytosis-lymphadenopathy plus syndrome
Reversed 0
HGVS NC_000010.10:g.73122094G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033097.3,