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rs397514626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397514626(C;C)
Make rs397514626(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position71351785
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs397514626
ebirs397514626
HLIrs397514626
Exacrs397514626
Varsomers397514626
Maprs397514626
PheGenIrs397514626
hapmaprs397514626
1000 genomesrs397514626
hgdprs397514626
ensemblrs397514626
gopubmedrs397514626
geneviewrs397514626
scholarrs397514626
googlers397514626
pharmgkbrs397514626
gwascentralrs397514626
openSNPrs397514626
23andMers397514626
23andMe allrs397514626
SNP Nexus

SNPshotrs397514626
SNPdbers397514626
MSV3drs397514626
GWAS Ctlgrs397514626
Max Magnitude0
ClinVar
Risk rs397514626(C;C)
Alt rs397514626(C;C)
Reference rs397514626(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.73111542T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000033098.3,