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rs61736892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61736892(A;A)
Make rs61736892(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position149498174
GeneIDS
is asnp
is mentioned by
dbSNPrs61736892
ebirs61736892
HLIrs61736892
Exacrs61736892
Varsomers61736892
Maprs61736892
PheGenIrs61736892
hapmaprs61736892
1000 genomesrs61736892
hgdprs61736892
ensemblrs61736892
gopubmedrs61736892
geneviewrs61736892
scholarrs61736892
googlers61736892
pharmgkbrs61736892
gwascentralrs61736892
openSNPrs61736892
23andMers61736892
23andMe allrs61736892
SNP Nexus

SNPshotrs61736892
SNPdbers61736892
MSV3drs61736892
GWAS Ctlgrs61736892
GMAF0.01451
Max Magnitude0
ClinVar
Risk rs61736892(A;A)
Alt rs61736892(A;A)
Reference rs61736892(G;G)
Significance Pathogenic
Disease not specified Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN not specified Mucopolysaccharidosis, MPS-II
Reversed 0
HGVS NC_000023.10:g.148579705G>A
CLNSRC ClinVar Emory University
CLNACC RCV000078368.4, RCV000205107.1,