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rs11090865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11090865(G;T)
Make rs11090865(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position46335792
GeneTRMU
is asnp
is mentioned by
dbSNPrs11090865
ebirs11090865
HLIrs11090865
Exacrs11090865
Varsomers11090865
Maprs11090865
PheGenIrs11090865
hapmaprs11090865
1000 genomesrs11090865
hgdprs11090865
ensemblrs11090865
gopubmedrs11090865
geneviewrs11090865
scholarrs11090865
googlers11090865
pharmgkbrs11090865
gwascentralrs11090865
openSNPrs11090865
23andMers11090865
23andMe allrs11090865
SNP Nexus

SNPshotrs11090865
SNPdbers11090865
MSV3drs11090865
GWAS Ctlgrs11090865
GMAF0.1088
Max Magnitude0
? (G;G) (G;T) (T;T) 28
OMIM610230
Desc
Variant0001
Relatedalso


ClinVar
Risk rs11090865(T;T)
Alt rs11090865(T;T)
Reference rs11090865(G;G)
Significance Other
Disease Deafness not specified
Variation info
Gene TRMU
CLNDBN Deafness, mitochondrial, modifier of not specified
Reversed 0
HGVS NC_000022.10:g.46731689G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001353.3, RCV000173461.2,



GET Evidence
TRMU-A10S
aa_change Ala10Ser
aa_change_short A10S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.134699
summary