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rs876657657

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657657(-;-)
Make rs876657657(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position17553478
GeneOTOG
is asnp
is mentioned by
dbSNPrs876657657
ebirs876657657
HLIrs876657657
Exacrs876657657
Varsomers876657657
Maprs876657657
PheGenIrs876657657
hapmaprs876657657
1000 genomesrs876657657
hgdprs876657657
ensemblrs876657657
gopubmedrs876657657
geneviewrs876657657
scholarrs876657657
googlers876657657
pharmgkbrs876657657
gwascentralrs876657657
openSNPrs876657657
23andMers876657657
23andMe allrs876657657
SNP Nexus

SNPshotrs876657657
SNPdbers876657657
MSV3drs876657657
GWAS Ctlgrs876657657
Max Magnitude0
ClinVar
Risk rs876657657(;)
Alt rs876657657(;)
Reference rs876657657(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOG
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000011.9:g.17575025delG
CLNSRC
CLNACC RCV000218007.1,