Have questions? Visit https://www.reddit.com/r/SNPedia

rs118204027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204027(C;T)
Make rs118204027(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position37724297
GeneTRIOBP
is asnp
is mentioned by
dbSNPrs118204027
ebirs118204027
HLIrs118204027
Exacrs118204027
Varsomers118204027
Maprs118204027
PheGenIrs118204027
hapmaprs118204027
1000 genomesrs118204027
hgdprs118204027
ensemblrs118204027
gopubmedrs118204027
geneviewrs118204027
scholarrs118204027
googlers118204027
pharmgkbrs118204027
gwascentralrs118204027
openSNPrs118204027
23andMers118204027
23andMe allrs118204027
SNP Nexus

SNPshotrs118204027
SNPdbers118204027
MSV3drs118204027
GWAS Ctlgrs118204027
Max Magnitude0
OMIM609761
Desc
Variant0002
Relatedalso
ClinVar
Risk rs118204027(T;T)
Alt rs118204027(T;T)
Reference rs118204027(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene TRIOBP
CLNDBN Deafness, autosomal recessive 28
Reversed 0
HGVS NC_000022.10:g.38120304C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001556.2,