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rs398122855

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122855(C;C)
Make rs398122855(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position107642384
GenePRPS1
is asnp
is mentioned by
dbSNPrs398122855
ebirs398122855
HLIrs398122855
Exacrs398122855
Varsomers398122855
Maprs398122855
PheGenIrs398122855
hapmaprs398122855
1000 genomesrs398122855
hgdprs398122855
ensemblrs398122855
gopubmedrs398122855
geneviewrs398122855
scholarrs398122855
googlers398122855
pharmgkbrs398122855
gwascentralrs398122855
openSNPrs398122855
23andMers398122855
23andMe allrs398122855
SNP Nexus

SNPshotrs398122855
SNPdbers398122855
MSV3drs398122855
GWAS Ctlgrs398122855
Max Magnitude0
ClinVar
Risk rs398122855(C;C)
Alt rs398122855(C;C)
Reference rs398122855(G;G)
Significance Pathogenic
Disease Arts syndrome
Variation info
Gene PRPS1
CLNDBN Arts syndrome
Reversed 0
HGVS NC_000023.10:g.106885614G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022882.3,