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rs118204029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204029(C;T)
Make rs118204029(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position37724918
GeneTRIOBP
is asnp
is mentioned by
dbSNPrs118204029
ebirs118204029
HLIrs118204029
Exacrs118204029
Varsomers118204029
Maprs118204029
PheGenIrs118204029
hapmaprs118204029
1000 genomesrs118204029
hgdprs118204029
ensemblrs118204029
gopubmedrs118204029
geneviewrs118204029
scholarrs118204029
googlers118204029
pharmgkbrs118204029
gwascentralrs118204029
openSNPrs118204029
23andMers118204029
23andMe allrs118204029
SNP Nexus

SNPshotrs118204029
SNPdbers118204029
MSV3drs118204029
GWAS Ctlgrs118204029
Max Magnitude0
OMIM609761
Desc
Variant0004
Relatedalso
ClinVar
Risk rs118204029(T;T)
Alt rs118204029(T;T)
Reference rs118204029(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene TRIOBP
CLNDBN Deafness, autosomal recessive 28
Reversed 0
HGVS NC_000022.10:g.38120925C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001558.2,