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rs864622774

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622774(C;T)
Make rs864622774(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149500987
GeneIDS
is asnp
is mentioned by
dbSNPrs864622774
ebirs864622774
HLIrs864622774
Exacrs864622774
Varsomers864622774
Maprs864622774
PheGenIrs864622774
hapmaprs864622774
1000 genomesrs864622774
hgdprs864622774
ensemblrs864622774
gopubmedrs864622774
geneviewrs864622774
scholarrs864622774
googlers864622774
pharmgkbrs864622774
gwascentralrs864622774
openSNPrs864622774
23andMers864622774
23andMe allrs864622774
SNP Nexus

SNPshotrs864622774
SNPdbers864622774
MSV3drs864622774
GWAS Ctlgrs864622774
Max Magnitude0
ClinVar
Risk rs864622774(T;T)
Alt rs864622774(T;T)
Reference rs864622774(C;C)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148582518G>A
CLNSRC
CLNACC RCV000205861.1,