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rs180177154

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177154(A;A)
Make rs180177154(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position107649991
GenePRPS1
is asnp
is mentioned by
dbSNPrs180177154
ebirs180177154
HLIrs180177154
Exacrs180177154
Varsomers180177154
Maprs180177154
PheGenIrs180177154
hapmaprs180177154
1000 genomesrs180177154
hgdprs180177154
ensemblrs180177154
gopubmedrs180177154
geneviewrs180177154
scholarrs180177154
googlers180177154
pharmgkbrs180177154
gwascentralrs180177154
openSNPrs180177154
23andMers180177154
23andMe allrs180177154
SNP Nexus

SNPshotrs180177154
SNPdbers180177154
MSV3drs180177154
GWAS Ctlgrs180177154
Max Magnitude0
ClinVar
Risk rs180177154(A;A)
Alt rs180177154(A;A)
Reference rs180177154(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene PRPS1
CLNDBN Deafness, X-linked 1
Reversed 0
HGVS NC_000023.10:g.106893221G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010618.3,