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rs876657716

From SNPedia

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Geno Mag Summary
(CTGCTT;CTGCTT) 0 common in clinvar
Make rs876657716(A;A)
Make rs876657716(A;CTGCTT)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position21697781
GeneOTOA
is asnp
is mentioned by
dbSNPrs876657716
ebirs876657716
HLIrs876657716
Exacrs876657716
Varsomers876657716
Maprs876657716
PheGenIrs876657716
hapmaprs876657716
1000 genomesrs876657716
hgdprs876657716
ensemblrs876657716
gopubmedrs876657716
geneviewrs876657716
scholarrs876657716
googlers876657716
pharmgkbrs876657716
gwascentralrs876657716
openSNPrs876657716
23andMers876657716
23andMe allrs876657716
SNP Nexus

SNPshotrs876657716
SNPdbers876657716
MSV3drs876657716
GWAS Ctlgrs876657716
Max Magnitude0
ClinVar
Risk rs876657716(A;A)
Alt rs876657716(A;A)
Reference rs876657716(CTGCTT;CTGCTT)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOA
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000016.9:g.21709102_21709107delinsA
CLNSRC
CLNACC RCV000222173.1,