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rs587781261

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781261(G;T)
Make rs587781261(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position107640932
GenePRPS1
is asnp
is mentioned by
dbSNPrs587781261
ebirs587781261
HLIrs587781261
Exacrs587781261
Varsomers587781261
Maprs587781261
PheGenIrs587781261
hapmaprs587781261
1000 genomesrs587781261
hgdprs587781261
ensemblrs587781261
gopubmedrs587781261
geneviewrs587781261
scholarrs587781261
googlers587781261
pharmgkbrs587781261
gwascentralrs587781261
openSNPrs587781261
23andMers587781261
23andMe allrs587781261
SNP Nexus

SNPshotrs587781261
SNPdbers587781261
MSV3drs587781261
GWAS Ctlgrs587781261
Max Magnitude0
ClinVar
Risk rs587781261(T;T)
Alt rs587781261(T;T)
Reference rs587781261(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene PRPS1
CLNDBN Deafness, X-linked 1
Reversed 0
HGVS NC_000023.10:g.106884162G>T
CLNSRC OMIM Allelic Variant VariO
CLNACC RCV000143857.2,