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rs138527651

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs138527651(C;C)
Make rs138527651(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position72821017
GeneTMC1
is asnp
is mentioned by
dbSNPrs138527651
ebirs138527651
HLIrs138527651
Exacrs138527651
Varsomers138527651
Maprs138527651
PheGenIrs138527651
hapmaprs138527651
1000 genomesrs138527651
hgdprs138527651
ensemblrs138527651
gopubmedrs138527651
geneviewrs138527651
scholarrs138527651
googlers138527651
pharmgkbrs138527651
gwascentralrs138527651
openSNPrs138527651
23andMers138527651
23andMe allrs138527651
SNP Nexus

SNPshotrs138527651
SNPdbers138527651
MSV3drs138527651
GWAS Ctlgrs138527651
Max Magnitude0
ClinVar
Risk rs138527651(C;C)
Alt rs138527651(C;C)
Reference rs138527651(T;T)
Significance Pathogenic
Disease Non-syndromic genetic deafness Deafness
Variation info
Gene TMC1
CLNDBN Non-syndromic genetic deafness Deafness, autosomal recessive 7
Reversed 0
HGVS NC_000009.11:g.75435933T>C
CLNSRC
CLNACC RCV000221167.1, RCV000225028.1, RCV000225055.1, RCV000225096.1, RCV000225097.1,