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rs118204028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204028(C;T)
Make rs118204028(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position37723445
GeneTRIOBP
is asnp
is mentioned by
dbSNPrs118204028
ebirs118204028
HLIrs118204028
Exacrs118204028
Varsomers118204028
Maprs118204028
PheGenIrs118204028
hapmaprs118204028
1000 genomesrs118204028
hgdprs118204028
ensemblrs118204028
gopubmedrs118204028
geneviewrs118204028
scholarrs118204028
googlers118204028
pharmgkbrs118204028
gwascentralrs118204028
openSNPrs118204028
23andMers118204028
23andMe allrs118204028
SNP Nexus

SNPshotrs118204028
SNPdbers118204028
MSV3drs118204028
GWAS Ctlgrs118204028
Max Magnitude0
OMIM609761
Desc
Variant0003
Relatedalso
ClinVar
Risk rs118204028(T;T)
Alt rs118204028(T;T)
Reference rs118204028(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene TRIOBP
CLNDBN Deafness, autosomal recessive 28
Reversed 0
HGVS NC_000022.10:g.38119452C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001557.2,