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rs387906708

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906708(G;T)
Make rs387906708(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position21737616
GeneSMPX
is asnp
is mentioned by
dbSNPrs387906708
ebirs387906708
HLIrs387906708
Exacrs387906708
Varsomers387906708
Maprs387906708
PheGenIrs387906708
hapmaprs387906708
1000 genomesrs387906708
hgdprs387906708
ensemblrs387906708
gopubmedrs387906708
geneviewrs387906708
scholarrs387906708
googlers387906708
pharmgkbrs387906708
gwascentralrs387906708
openSNPrs387906708
23andMers387906708
23andMe allrs387906708
SNP Nexus

SNPshotrs387906708
SNPdbers387906708
MSV3drs387906708
GWAS Ctlgrs387906708
Max Magnitude0
ClinVar
Risk rs387906708(T;T)
Alt rs387906708(T;T)
Reference rs387906708(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene SMPX
CLNDBN Deafness, X-linked 4
Reversed 1
HGVS NC_000023.10:g.21755734C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022839.21,