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rs193302912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193302912(A;A)
Make rs193302912(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position149490385
GeneIDS
is asnp
is mentioned by
dbSNPrs193302912
ebirs193302912
HLIrs193302912
Exacrs193302912
Varsomers193302912
Maprs193302912
PheGenIrs193302912
hapmaprs193302912
1000 genomesrs193302912
hgdprs193302912
ensemblrs193302912
gopubmedrs193302912
geneviewrs193302912
scholarrs193302912
googlers193302912
pharmgkbrs193302912
gwascentralrs193302912
openSNPrs193302912
23andMers193302912
23andMe allrs193302912
SNP Nexus

SNPshotrs193302912
SNPdbers193302912
MSV3drs193302912
GWAS Ctlgrs193302912
Max Magnitude0
ClinVar
Risk rs193302912(A;A)
Alt rs193302912(A;A)
Reference rs193302912(G;G)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148571916C>T
CLNSRC
CLNACC RCV000205196.1,