Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044671

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044671(-;C)
Make rs797044671(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position149504188
GeneIDS
is asnp
is mentioned by
dbSNPrs797044671
dbSNP (old)rs797044671
ClinGenrs797044671
ebirs797044671
HLIrs797044671
Exacrs797044671
Gnomadrs797044671
Varsomers797044671
Maprs797044671
PheGenIrs797044671
Biobankrs797044671
1000 genomesrs797044671
hgdprs797044671
ensemblrs797044671
gopubmedrs797044671
geneviewrs797044671
scholarrs797044671
googlers797044671
pharmgkbrs797044671
gwascentralrs797044671
openSNPrs797044671
23andMers797044671
23andMe allrs797044671
SNP Nexus

SNPshotrs797044671
SNPdbers797044671
MSV3drs797044671
GWAS Ctlgrs797044671
Max Magnitude0
ClinVar
Risk rs797044671(C;C)
Alt rs797044671(C;C)
Reference Rs797044671(-;-)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene IDS
CLNDBN Mucopolysaccharidosis, MPS-II
Reversed 1
HGVS NC_000023.10:g.148585719dupG
CLNSRC
CLNACC RCV000175548.1,