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rs869025308

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025308(G;T)
Make rs869025308(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149490313
GeneIDS
is asnp
is mentioned by
dbSNPrs869025308
ebirs869025308
HLIrs869025308
Exacrs869025308
Varsomers869025308
Maprs869025308
PheGenIrs869025308
hapmaprs869025308
1000 genomesrs869025308
hgdprs869025308
ensemblrs869025308
gopubmedrs869025308
geneviewrs869025308
scholarrs869025308
googlers869025308
pharmgkbrs869025308
gwascentralrs869025308
openSNPrs869025308
23andMers869025308
23andMe allrs869025308
SNP Nexus

SNPshotrs869025308
SNPdbers869025308
MSV3drs869025308
GWAS Ctlgrs869025308
Max Magnitude0
ClinVar
Risk rs869025308(T;T)
Alt rs869025308(T;T)
Reference rs869025308(G;G)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148571844C>A
CLNSRC
CLNACC RCV000207409.1,