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rs876657658

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs876657658(-;-)
Make rs876657658(-;AT)
Make rs876657658(AT;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position80238874
GeneOTOGL
is asnp
is mentioned by
dbSNPrs876657658
ebirs876657658
HLIrs876657658
Exacrs876657658
Varsomers876657658
Maprs876657658
PheGenIrs876657658
hapmaprs876657658
1000 genomesrs876657658
hgdprs876657658
ensemblrs876657658
gopubmedrs876657658
geneviewrs876657658
scholarrs876657658
googlers876657658
pharmgkbrs876657658
gwascentralrs876657658
openSNPrs876657658
23andMers876657658
23andMe allrs876657658
SNP Nexus

SNPshotrs876657658
SNPdbers876657658
MSV3drs876657658
GWAS Ctlgrs876657658
Max Magnitude0
ClinVar
Risk rs876657658(;)
Alt rs876657658(;)
Reference rs876657658(TA;TA)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOGL
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000012.11:g.80632654_80632655delAT
CLNSRC
CLNACC RCV000220106.1,