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rs864622779

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622779(C;C)
Make rs864622779(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149498202
GeneIDS
is asnp
is mentioned by
dbSNPrs864622779
ebirs864622779
HLIrs864622779
Exacrs864622779
Varsomers864622779
Maprs864622779
PheGenIrs864622779
hapmaprs864622779
1000 genomesrs864622779
hgdprs864622779
ensemblrs864622779
gopubmedrs864622779
geneviewrs864622779
scholarrs864622779
googlers864622779
pharmgkbrs864622779
gwascentralrs864622779
openSNPrs864622779
23andMers864622779
23andMe allrs864622779
SNP Nexus

SNPshotrs864622779
SNPdbers864622779
MSV3drs864622779
GWAS Ctlgrs864622779
Max Magnitude0
ClinVar
Risk rs864622779(C;C)
Alt rs864622779(C;C)
Reference rs864622779(G;G)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148579733C>G
CLNSRC
CLNACC RCV000204533.1,