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rs869025303

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025303(A;C)
Make rs869025303(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149487080
GeneIDS
is asnp
is mentioned by
dbSNPrs869025303
ebirs869025303
HLIrs869025303
Exacrs869025303
Varsomers869025303
Maprs869025303
PheGenIrs869025303
hapmaprs869025303
1000 genomesrs869025303
hgdprs869025303
ensemblrs869025303
gopubmedrs869025303
geneviewrs869025303
scholarrs869025303
googlers869025303
pharmgkbrs869025303
gwascentralrs869025303
openSNPrs869025303
23andMers869025303
23andMe allrs869025303
SNP Nexus

SNPshotrs869025303
SNPdbers869025303
MSV3drs869025303
GWAS Ctlgrs869025303
Max Magnitude0
ClinVar
Risk rs869025303(C;C)
Alt rs869025303(C;C)
Reference rs869025303(A;A)
Significance Probable-Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148568611T>G
CLNSRC
CLNACC RCV000207405.1,