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rs387906706

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906706(G;T)
Make rs387906706(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position21737655
GeneSMPX
is asnp
is mentioned by
dbSNPrs387906706
ebirs387906706
HLIrs387906706
Exacrs387906706
Varsomers387906706
Maprs387906706
PheGenIrs387906706
hapmaprs387906706
1000 genomesrs387906706
hgdprs387906706
ensemblrs387906706
gopubmedrs387906706
geneviewrs387906706
scholarrs387906706
googlers387906706
pharmgkbrs387906706
gwascentralrs387906706
openSNPrs387906706
23andMers387906706
23andMe allrs387906706
SNP Nexus

SNPshotrs387906706
SNPdbers387906706
MSV3drs387906706
GWAS Ctlgrs387906706
Max Magnitude0
ClinVar
Risk rs387906706(T;T)
Alt rs387906706(T;T)
Reference rs387906706(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene SMPX
CLNDBN Deafness, X-linked 4
Reversed 1
HGVS NC_000023.10:g.21755773C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022837.24,