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rs121912584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912584(A;A)
Make rs121912584(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71362489
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs121912584
ebirs121912584
HLIrs121912584
Exacrs121912584
Varsomers121912584
Maprs121912584
PheGenIrs121912584
hapmaprs121912584
1000 genomesrs121912584
hgdprs121912584
ensemblrs121912584
gopubmedrs121912584
geneviewrs121912584
scholarrs121912584
googlers121912584
pharmgkbrs121912584
gwascentralrs121912584
openSNPrs121912584
23andMers121912584
23andMe allrs121912584
SNP Nexus

SNPshotrs121912584
SNPdbers121912584
MSV3drs121912584
GWAS Ctlgrs121912584
Max Magnitude0
OMIM612373
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912584(A;A)
Alt rs121912584(A;A)
Reference rs121912584(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.73122246G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000595.3,