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

rs1300268466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 3 Carrier of a DFNB7/11 deafness mutation
(C;T) 3 Carrier of a DFNB7/11 deafness mutation
(T;T) 0 common/normal


Make rs1300268466(C;C)
ReferenceGRCh38.p7 38.3/151
Chromosome9
Position72688758
GeneTMC1
is asnp
is mentioned by
dbSNPrs1300268466
dbSNP (classic)rs1300268466
ClinGenrs1300268466
ebirs1300268466
HLIrs1300268466
Exacrs1300268466
Gnomadrs1300268466
Varsomers1300268466
LitVarrs1300268466
Maprs1300268466
PheGenIrs1300268466
Biobankrs1300268466
1000 genomesrs1300268466
hgdprs1300268466
ensemblrs1300268466
geneviewrs1300268466
scholarrs1300268466
googlers1300268466
pharmgkbrs1300268466
gwascentralrs1300268466
openSNPrs1300268466
23andMers1300268466
SNPshotrs1300268466
SNPdbers1300268466
MSV3drs1300268466
GWAS Ctlgrs1300268466
Max Magnitude3