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rs869025306

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs869025306(-;-)
Make rs869025306(-;TT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149486972
GeneIDS
is asnp
is mentioned by
dbSNPrs869025306
ebirs869025306
HLIrs869025306
Exacrs869025306
Varsomers869025306
Maprs869025306
PheGenIrs869025306
hapmaprs869025306
1000 genomesrs869025306
hgdprs869025306
ensemblrs869025306
gopubmedrs869025306
geneviewrs869025306
scholarrs869025306
googlers869025306
pharmgkbrs869025306
gwascentralrs869025306
openSNPrs869025306
23andMers869025306
23andMe allrs869025306
SNP Nexus

SNPshotrs869025306
SNPdbers869025306
MSV3drs869025306
GWAS Ctlgrs869025306
Max Magnitude0
ClinVar
Risk rs869025306(;)
Alt rs869025306(;)
Reference rs869025306(TT;TT)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148568503_148568504delAA
CLNSRC
CLNACC RCV000207401.1,