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rs1060499809

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499809(C;T)
Make rs1060499809(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position37724003
GeneTRIOBP
is asnp
is mentioned by
dbSNPrs1060499809
dbSNP (old)rs1060499809
ClinGenrs1060499809
ebirs1060499809
HLIrs1060499809
Exacrs1060499809
Gnomadrs1060499809
Varsomers1060499809
Maprs1060499809
PheGenIrs1060499809
Biobankrs1060499809
1000 genomesrs1060499809
hgdprs1060499809
ensemblrs1060499809
gopubmedrs1060499809
geneviewrs1060499809
scholarrs1060499809
googlers1060499809
pharmgkbrs1060499809
gwascentralrs1060499809
openSNPrs1060499809
23andMers1060499809
23andMe allrs1060499809
SNPshotrs1060499809
SNPdbers1060499809
MSV3drs1060499809
GWAS Ctlgrs1060499809
Max Magnitude0
ClinVar
Risk rs1060499809(T;T)
Alt rs1060499809(T;T)
Reference Rs1060499809(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene TRIOBP
CLNDBN Deafness, autosomal recessive 28
Reversed 0
HGVS NC_000022.10:g.38120010C>T
CLNSRC
CLNACC RCV000454233.1,