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rs267607135

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607135(A;A)
Make rs267607135(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137199473
GeneTPRN
is asnp
is mentioned by
dbSNPrs267607135
ebirs267607135
HLIrs267607135
Exacrs267607135
Varsomers267607135
Maprs267607135
PheGenIrs267607135
hapmaprs267607135
1000 genomesrs267607135
hgdprs267607135
ensemblrs267607135
gopubmedrs267607135
geneviewrs267607135
scholarrs267607135
googlers267607135
pharmgkbrs267607135
gwascentralrs267607135
openSNPrs267607135
23andMers267607135
23andMe allrs267607135
SNP Nexus

SNPshotrs267607135
SNPdbers267607135
MSV3drs267607135
GWAS Ctlgrs267607135
Max Magnitude0
ClinVar
Risk rs267607135(A;A)
Alt rs267607135(A;A)
Reference rs267607135(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene TPRN
CLNDBN Deafness, autosomal recessive 79
Reversed 1
HGVS NC_000009.11:g.140093925C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000157.2,