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rs869025301

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025301(C;C)
Make rs869025301(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149504264
GeneIDS
is asnp
is mentioned by
dbSNPrs869025301
ebirs869025301
HLIrs869025301
Exacrs869025301
Varsomers869025301
Maprs869025301
PheGenIrs869025301
hapmaprs869025301
1000 genomesrs869025301
hgdprs869025301
ensemblrs869025301
gopubmedrs869025301
geneviewrs869025301
scholarrs869025301
googlers869025301
pharmgkbrs869025301
gwascentralrs869025301
openSNPrs869025301
23andMers869025301
23andMe allrs869025301
SNP Nexus

SNPshotrs869025301
SNPdbers869025301
MSV3drs869025301
GWAS Ctlgrs869025301
Max Magnitude0
ClinVar
Risk rs869025301(C;C)
Alt rs869025301(C;C)
Reference rs869025301(G;G)
Significance Probable-Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148585794C>G
CLNSRC
CLNACC RCV000207419.1,