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rs267607057

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607057(G;G)
Make rs267607057(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position71344255
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs267607057
ebirs267607057
HLIrs267607057
Exacrs267607057
Varsomers267607057
Maprs267607057
PheGenIrs267607057
hapmaprs267607057
1000 genomesrs267607057
hgdprs267607057
ensemblrs267607057
gopubmedrs267607057
geneviewrs267607057
scholarrs267607057
googlers267607057
pharmgkbrs267607057
gwascentralrs267607057
openSNPrs267607057
23andMers267607057
23andMe allrs267607057
SNP Nexus

SNPshotrs267607057
SNPdbers267607057
MSV3drs267607057
GWAS Ctlgrs267607057
Max Magnitude0
ClinVar
Risk rs267607057(G;G)
Alt rs267607057(G;G)
Reference rs267607057(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.73104012T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000598.2,