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rs876657656

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657656(-;-)
Make rs876657656(-;ACTGGACACCCA)
Make rs876657656(ACTGGACACCCA;ACTGGACACCCA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position17574879
GeneOTOG
is asnp
is mentioned by
dbSNPrs876657656
ebirs876657656
HLIrs876657656
Exacrs876657656
Varsomers876657656
Maprs876657656
PheGenIrs876657656
hapmaprs876657656
1000 genomesrs876657656
hgdprs876657656
ensemblrs876657656
gopubmedrs876657656
geneviewrs876657656
scholarrs876657656
googlers876657656
pharmgkbrs876657656
gwascentralrs876657656
openSNPrs876657656
23andMers876657656
23andMe allrs876657656
SNP Nexus

SNPshotrs876657656
SNPdbers876657656
MSV3drs876657656
GWAS Ctlgrs876657656
Max Magnitude0
ClinVar
Risk rs876657656(AACTGGACACCC;AACTGGACACCC)
Alt rs876657656(AACTGGACACCC;AACTGGACACCC)
Reference rs876657656(;)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOG
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000011.9:g.17596426_17596427insACTGGACACCCA
CLNSRC
CLNACC RCV000214336.1,