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rs121912583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912583(A;A)
Make rs121912583(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71362459
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs121912583
ebirs121912583
HLIrs121912583
Exacrs121912583
Varsomers121912583
Maprs121912583
PheGenIrs121912583
hapmaprs121912583
1000 genomesrs121912583
hgdprs121912583
ensemblrs121912583
gopubmedrs121912583
geneviewrs121912583
scholarrs121912583
googlers121912583
pharmgkbrs121912583
gwascentralrs121912583
openSNPrs121912583
23andMers121912583
23andMe allrs121912583
SNP Nexus

SNPshotrs121912583
SNPdbers121912583
MSV3drs121912583
GWAS Ctlgrs121912583
Max Magnitude0
OMIM612373
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912583(A;A)
Alt rs121912583(A;A)
Reference rs121912583(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.73122216G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000593.2,