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rs864622778

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622778(A;A)
Make rs864622778(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149498106
GeneIDS
is asnp
is mentioned by
dbSNPrs864622778
ebirs864622778
HLIrs864622778
Exacrs864622778
Varsomers864622778
Maprs864622778
PheGenIrs864622778
hapmaprs864622778
1000 genomesrs864622778
hgdprs864622778
ensemblrs864622778
gopubmedrs864622778
geneviewrs864622778
scholarrs864622778
googlers864622778
pharmgkbrs864622778
gwascentralrs864622778
openSNPrs864622778
23andMers864622778
23andMe allrs864622778
SNP Nexus

SNPshotrs864622778
SNPdbers864622778
MSV3drs864622778
GWAS Ctlgrs864622778
Max Magnitude0
ClinVar
Risk rs864622778(A;A)
Alt rs864622778(A;A)
Reference rs864622778(G;G)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148579637C>T
CLNSRC
CLNACC RCV000204551.1,