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rs1060499590

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499590(A;A)
Make rs1060499590(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position21737698
GeneSMPX
is asnp
is mentioned by
dbSNPrs1060499590
dbSNP (old)rs1060499590
ClinGenrs1060499590
ebirs1060499590
HLIrs1060499590
Exacrs1060499590
Gnomadrs1060499590
Varsomers1060499590
Maprs1060499590
PheGenIrs1060499590
Biobankrs1060499590
1000 genomesrs1060499590
hgdprs1060499590
ensemblrs1060499590
gopubmedrs1060499590
geneviewrs1060499590
scholarrs1060499590
googlers1060499590
pharmgkbrs1060499590
gwascentralrs1060499590
openSNPrs1060499590
23andMers1060499590
23andMe allrs1060499590
SNPshotrs1060499590
SNPdbers1060499590
MSV3drs1060499590
GWAS Ctlgrs1060499590
Max Magnitude0
ClinVar
Risk rs1060499590(A;A)
Alt rs1060499590(A;A)
Reference Rs1060499590(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene SMPX
CLNDBN Deafness, X-linked 4
Reversed 1
HGVS NC_000023.10:g.21755816C>T
CLNSRC
CLNACC RCV000477909.1,