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rs757327146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;G) 3 Carrier of a DFNB7/11 deafness mutation
Make rs757327146(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome9
Position72789236
GeneTMC1
is asnp
is mentioned by
dbSNPrs757327146
dbSNP (classic)rs757327146
ClinGenrs757327146
ebirs757327146
HLIrs757327146
Exacrs757327146
Gnomadrs757327146
Varsomers757327146
LitVarrs757327146
Maprs757327146
PheGenIrs757327146
Biobankrs757327146
1000 genomesrs757327146
hgdprs757327146
ensemblrs757327146
geneviewrs757327146
scholarrs757327146
googlers757327146
pharmgkbrs757327146
gwascentralrs757327146
openSNPrs757327146
23andMers757327146
SNPshotrs757327146
SNPdbers757327146
MSV3drs757327146
GWAS Ctlgrs757327146
Max Magnitude3