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rs118204026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204026(C;T)
Make rs118204026(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position37723595
GeneTRIOBP
is asnp
is mentioned by
dbSNPrs118204026
ebirs118204026
HLIrs118204026
Exacrs118204026
Varsomers118204026
Maprs118204026
PheGenIrs118204026
hapmaprs118204026
1000 genomesrs118204026
hgdprs118204026
ensemblrs118204026
gopubmedrs118204026
geneviewrs118204026
scholarrs118204026
googlers118204026
pharmgkbrs118204026
gwascentralrs118204026
openSNPrs118204026
23andMers118204026
23andMe allrs118204026
SNP Nexus

SNPshotrs118204026
SNPdbers118204026
MSV3drs118204026
GWAS Ctlgrs118204026
Max Magnitude0
OMIM609761
Desc
Variant0001
Relatedalso
ClinVar
Risk rs118204026(G,T;G,T)
Alt rs118204026(G,T;G,T)
Reference rs118204026(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene TRIOBP
CLNDBN Deafness, autosomal recessive 28
Reversed 0
HGVS NC_000022.10:g.38119602C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001555.2,