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rs876657727

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657727(-;-)
Make rs876657727(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position72791897
GeneTMC1
is asnp
is mentioned by
dbSNPrs876657727
ebirs876657727
HLIrs876657727
Exacrs876657727
Varsomers876657727
Maprs876657727
PheGenIrs876657727
hapmaprs876657727
1000 genomesrs876657727
hgdprs876657727
ensemblrs876657727
gopubmedrs876657727
geneviewrs876657727
scholarrs876657727
googlers876657727
pharmgkbrs876657727
gwascentralrs876657727
openSNPrs876657727
23andMers876657727
23andMe allrs876657727
SNP Nexus

SNPshotrs876657727
SNPdbers876657727
MSV3drs876657727
GWAS Ctlgrs876657727
Max Magnitude0
ClinVar
Risk rs876657727(;)
Alt rs876657727(;)
Reference rs876657727(T;T)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene TMC1
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000009.11:g.75406813delT
CLNSRC
CLNACC RCV000217598.1,