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rs180177151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177151(A;A)
Make rs180177151(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position107639365
GenePRPS1
is asnp
is mentioned by
dbSNPrs180177151
ebirs180177151
HLIrs180177151
Exacrs180177151
Varsomers180177151
Maprs180177151
PheGenIrs180177151
hapmaprs180177151
1000 genomesrs180177151
hgdprs180177151
ensemblrs180177151
gopubmedrs180177151
geneviewrs180177151
scholarrs180177151
googlers180177151
pharmgkbrs180177151
gwascentralrs180177151
openSNPrs180177151
23andMers180177151
23andMe allrs180177151
SNP Nexus

SNPshotrs180177151
SNPdbers180177151
MSV3drs180177151
GWAS Ctlgrs180177151
Max Magnitude0
ClinVar
Risk rs180177151(A;A)
Alt rs180177151(A;A)
Reference rs180177151(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene PRPS1
CLNDBN Deafness, X-linked 1
Reversed 0
HGVS NC_000023.10:g.106882595G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010616.3,