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rs267607058

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607058(C;G)
Make rs267607058(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71362526
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs267607058
ebirs267607058
HLIrs267607058
Exacrs267607058
Varsomers267607058
Maprs267607058
PheGenIrs267607058
hapmaprs267607058
1000 genomesrs267607058
hgdprs267607058
ensemblrs267607058
gopubmedrs267607058
geneviewrs267607058
scholarrs267607058
googlers267607058
pharmgkbrs267607058
gwascentralrs267607058
openSNPrs267607058
23andMers267607058
23andMe allrs267607058
SNP Nexus

SNPshotrs267607058
SNPdbers267607058
MSV3drs267607058
GWAS Ctlgrs267607058
Max Magnitude0
ClinVar
Risk rs267607058(G,T;G,T)
Alt rs267607058(G,T;G,T)
Reference rs267607058(C;C)
Significance Pathogenic
Disease Histiocytosis-lymphadenopathy plus syndrome
Variation info
Gene SLC29A3
CLNDBN Histiocytosis-lymphadenopathy plus syndrome
Reversed 0
HGVS NC_000010.10:g.73122283C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000599.2,