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rs267607056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607056(G;T)
Make rs267607056(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position71362510
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs267607056
ebirs267607056
HLIrs267607056
Exacrs267607056
Varsomers267607056
Maprs267607056
PheGenIrs267607056
hapmaprs267607056
1000 genomesrs267607056
hgdprs267607056
ensemblrs267607056
gopubmedrs267607056
geneviewrs267607056
scholarrs267607056
googlers267607056
pharmgkbrs267607056
gwascentralrs267607056
openSNPrs267607056
23andMers267607056
23andMe allrs267607056
SNP Nexus

SNPshotrs267607056
SNPdbers267607056
MSV3drs267607056
GWAS Ctlgrs267607056
Max Magnitude0
ClinVar
Risk rs267607056(T;T)
Alt rs267607056(T;T)
Reference rs267607056(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.73122267G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000594.2,