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rs876657728

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657728(A;A)
Make rs876657728(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position72805491
GeneTMC1
is asnp
is mentioned by
dbSNPrs876657728
ebirs876657728
HLIrs876657728
Exacrs876657728
Varsomers876657728
Maprs876657728
PheGenIrs876657728
hapmaprs876657728
1000 genomesrs876657728
hgdprs876657728
ensemblrs876657728
gopubmedrs876657728
geneviewrs876657728
scholarrs876657728
googlers876657728
pharmgkbrs876657728
gwascentralrs876657728
openSNPrs876657728
23andMers876657728
23andMe allrs876657728
SNP Nexus

SNPshotrs876657728
SNPdbers876657728
MSV3drs876657728
GWAS Ctlgrs876657728
Max Magnitude0
ClinVar
Risk rs876657728(A;A)
Alt rs876657728(A;A)
Reference rs876657728(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene TMC1
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000009.11:g.75420407G>A
CLNSRC
CLNACC RCV000219905.1,