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rs587780463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780463(A;A)
Make rs587780463(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position71323055
GeneSLC29A3
is asnp
is mentioned by
dbSNPrs587780463
dbSNP (classic)rs587780463
ClinGenrs587780463
ebirs587780463
HLIrs587780463
Exacrs587780463
Gnomadrs587780463
Varsomers587780463
LitVarrs587780463
Maprs587780463
PheGenIrs587780463
Biobankrs587780463
1000 genomesrs587780463
hgdprs587780463
ensemblrs587780463
geneviewrs587780463
scholarrs587780463
googlers587780463
pharmgkbrs587780463
gwascentralrs587780463
openSNPrs587780463
23andMers587780463
SNPshotrs587780463
SNPdbers587780463
MSV3drs587780463
GWAS Ctlgrs587780463
Max Magnitude0
ClinVar
Risk rs587780463(A;A) rs587780463(C;C)
Alt rs587780463(A;A) rs587780463(C;C)
Reference Rs587780463(G;G)
Significance Pathogenic
Disease Histiocytosis-lymphadenopathy plus syndrome not provided
Variation info
Gene SLC29A3
CLNDBN Histiocytosis-lymphadenopathy plus syndrome not provided
Reversed 0
HGVS NC_000010.10:g.73082812G>A; NC_000010.10:g.73082812G>C
CLNSRC
CLNACC RCV000118377.1, RCV000489914.1,