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rs879255246

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255246(C;C)
Make rs879255246(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position26484568
GeneOTOF
is asnp
is mentioned by
dbSNPrs879255246
ebirs879255246
HLIrs879255246
Exacrs879255246
Varsomers879255246
Maprs879255246
PheGenIrs879255246
hapmaprs879255246
1000 genomesrs879255246
hgdprs879255246
ensemblrs879255246
gopubmedrs879255246
geneviewrs879255246
scholarrs879255246
googlers879255246
pharmgkbrs879255246
gwascentralrs879255246
openSNPrs879255246
23andMers879255246
23andMe allrs879255246
SNP Nexus

SNPshotrs879255246
SNPdbers879255246
MSV3drs879255246
GWAS Ctlgrs879255246
Max Magnitude0
ClinVar
Risk rs879255246(C;C)
Alt rs879255246(C;C)
Reference rs879255246(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive
Reversed 1
HGVS NC_000002.11:g.26707436C>G
CLNSRC
CLNACC RCV000239359.1,