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rs781997631

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs781997631(A;G)
Make rs781997631(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149504206
GeneIDS
is asnp
is mentioned by
dbSNPrs781997631
ebirs781997631
HLIrs781997631
Exacrs781997631
Varsomers781997631
Maprs781997631
PheGenIrs781997631
hapmaprs781997631
1000 genomesrs781997631
hgdprs781997631
ensemblrs781997631
gopubmedrs781997631
geneviewrs781997631
scholarrs781997631
googlers781997631
pharmgkbrs781997631
gwascentralrs781997631
openSNPrs781997631
23andMers781997631
23andMe allrs781997631
SNP Nexus

SNPshotrs781997631
SNPdbers781997631
MSV3drs781997631
GWAS Ctlgrs781997631
Max Magnitude0
ClinVar
Risk rs781997631(G;G)
Alt rs781997631(G;G)
Reference rs781997631(A;A)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 0
HGVS NC_000023.10:g.148585736A>T
CLNSRC
CLNACC RCV000206626.1,