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rs387907067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907067(C;T)
Make rs387907067(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position71362267
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs387907067
ebirs387907067
HLIrs387907067
Exacrs387907067
Varsomers387907067
Maprs387907067
PheGenIrs387907067
hapmaprs387907067
1000 genomesrs387907067
hgdprs387907067
ensemblrs387907067
gopubmedrs387907067
geneviewrs387907067
scholarrs387907067
googlers387907067
pharmgkbrs387907067
gwascentralrs387907067
openSNPrs387907067
23andMers387907067
23andMe allrs387907067
SNP Nexus

SNPshotrs387907067
SNPdbers387907067
MSV3drs387907067
GWAS Ctlgrs387907067
Max Magnitude0
ClinVar
Risk rs387907067(T;T)
Alt rs387907067(T;T)
Reference rs387907067(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.73122024C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023939.2,