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rs876657661

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657661(A;T)
Make rs876657661(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position121189078
GeneTECTA
is asnp
is mentioned by
dbSNPrs876657661
ebirs876657661
HLIrs876657661
Exacrs876657661
Varsomers876657661
Maprs876657661
PheGenIrs876657661
hapmaprs876657661
1000 genomesrs876657661
hgdprs876657661
ensemblrs876657661
gopubmedrs876657661
geneviewrs876657661
scholarrs876657661
googlers876657661
pharmgkbrs876657661
gwascentralrs876657661
openSNPrs876657661
23andMers876657661
23andMe allrs876657661
SNP Nexus

SNPshotrs876657661
SNPdbers876657661
MSV3drs876657661
GWAS Ctlgrs876657661
Max Magnitude0
ClinVar
Risk rs876657661(T;T)
Alt rs876657661(T;T)
Reference rs876657661(A;A)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene TECTA
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000011.9:g.121059787A>T
CLNSRC
CLNACC RCV000214219.1,