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rs1064797096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome5
Position141524179
GeneDIAPH1
is asnp
is mentioned by
dbSNPrs1064797096
dbSNP (old)rs1064797096
ClinGenrs1064797096
ebirs1064797096
HLIrs1064797096
Exacrs1064797096
Gnomadrs1064797096
Varsomers1064797096
Maprs1064797096
PheGenIrs1064797096
Biobankrs1064797096
1000 genomesrs1064797096
hgdprs1064797096
ensemblrs1064797096
gopubmedrs1064797096
geneviewrs1064797096
scholarrs1064797096
googlers1064797096
pharmgkbrs1064797096
gwascentralrs1064797096
openSNPrs1064797096
23andMers1064797096
23andMe allrs1064797096
SNPshotrs1064797096
SNPdbers1064797096
MSV3drs1064797096
GWAS Ctlgrs1064797096
Max Magnitude0
ClinVar
Risk rs1064797096(-;-)
Alt rs1064797096(-;-)
Reference Rs1064797096(AG;AG)
Significance Pathogenic
Disease Deafness
Variation info
Gene DIAPH1
CLNDBN Deafness, autosomal dominant 1
Reversed 1
HGVS NC_000005.9:g.140903746_140903747delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000488304.1,