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rs387906707

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906707(G;T)
Make rs387906707(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position21743773
GeneSMPX
is asnp
is mentioned by
dbSNPrs387906707
ebirs387906707
HLIrs387906707
Exacrs387906707
Varsomers387906707
Maprs387906707
PheGenIrs387906707
hapmaprs387906707
1000 genomesrs387906707
hgdprs387906707
ensemblrs387906707
gopubmedrs387906707
geneviewrs387906707
scholarrs387906707
googlers387906707
pharmgkbrs387906707
gwascentralrs387906707
openSNPrs387906707
23andMers387906707
23andMe allrs387906707
SNP Nexus

SNPshotrs387906707
SNPdbers387906707
MSV3drs387906707
GWAS Ctlgrs387906707
Max Magnitude0
ClinVar
Risk rs387906707(T;T)
Alt rs387906707(T;T)
Reference rs387906707(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene SMPX
CLNDBN Deafness, X-linked 4
Reversed 1
HGVS NC_000023.10:g.21761891C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022838.11,