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rs387907066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907066(A;A)
Make rs387907066(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71362268
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs387907066
ebirs387907066
HLIrs387907066
Exacrs387907066
Varsomers387907066
Maprs387907066
PheGenIrs387907066
hapmaprs387907066
1000 genomesrs387907066
hgdprs387907066
ensemblrs387907066
gopubmedrs387907066
geneviewrs387907066
scholarrs387907066
googlers387907066
pharmgkbrs387907066
gwascentralrs387907066
openSNPrs387907066
23andMers387907066
23andMe allrs387907066
SNP Nexus

SNPshotrs387907066
SNPdbers387907066
MSV3drs387907066
GWAS Ctlgrs387907066
Max Magnitude0
ClinVar
Risk rs387907066(A;A)
Alt rs387907066(A;A)
Reference rs387907066(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.73122025G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023938.3,