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rs760574657

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760574657(C;T)
Make rs760574657(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position121168903
GeneTECTA
is asnp
is mentioned by
dbSNPrs760574657
ebirs760574657
HLIrs760574657
Exacrs760574657
Varsomers760574657
Maprs760574657
PheGenIrs760574657
hapmaprs760574657
1000 genomesrs760574657
hgdprs760574657
ensemblrs760574657
gopubmedrs760574657
geneviewrs760574657
scholarrs760574657
googlers760574657
pharmgkbrs760574657
gwascentralrs760574657
openSNPrs760574657
23andMers760574657
23andMe allrs760574657
SNP Nexus

SNPshotrs760574657
SNPdbers760574657
MSV3drs760574657
GWAS Ctlgrs760574657
Max Magnitude0
ClinVar
Risk rs760574657(T;T)
Alt rs760574657(T;T)
Reference rs760574657(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene TECTA
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000011.9:g.121039612C>T
CLNSRC
CLNACC RCV000220688.1,