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rs267607120

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607120(A;A)
Make rs267607120(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position46705866
GeneTMIE
is asnp
is mentioned by
dbSNPrs267607120
ebirs267607120
HLIrs267607120
Exacrs267607120
Varsomers267607120
Maprs267607120
PheGenIrs267607120
hapmaprs267607120
1000 genomesrs267607120
hgdprs267607120
ensemblrs267607120
gopubmedrs267607120
geneviewrs267607120
scholarrs267607120
googlers267607120
pharmgkbrs267607120
gwascentralrs267607120
openSNPrs267607120
23andMers267607120
23andMe allrs267607120
SNP Nexus

SNPshotrs267607120
SNPdbers267607120
MSV3drs267607120
GWAS Ctlgrs267607120
Max Magnitude0
ClinVar
Risk rs267607120(A;A)
Alt rs267607120(A;A)
Reference rs267607120(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene TMIE
CLNDBN Deafness, autosomal recessive 6
Reversed 0
HGVS NC_000003.11:g.46747356G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003561.4,