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rs1057518840

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518840(A;G)
Make rs1057518840(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position26476319
GeneOTOF
is asnp
is mentioned by
dbSNPrs1057518840
dbSNP (old)rs1057518840
ClinGenrs1057518840
ebirs1057518840
HLIrs1057518840
Exacrs1057518840
Gnomadrs1057518840
Varsomers1057518840
Maprs1057518840
PheGenIrs1057518840
Biobankrs1057518840
1000 genomesrs1057518840
hgdprs1057518840
ensemblrs1057518840
gopubmedrs1057518840
geneviewrs1057518840
scholarrs1057518840
googlers1057518840
pharmgkbrs1057518840
gwascentralrs1057518840
openSNPrs1057518840
23andMers1057518840
23andMe allrs1057518840
SNPshotrs1057518840
SNPdbers1057518840
MSV3drs1057518840
GWAS Ctlgrs1057518840
Max Magnitude0
ClinVar
Risk rs1057518840(G;G)
Alt rs1057518840(G;G)
Reference Rs1057518840(A;A)
Significance Probable-Pathogenic
Disease Hearing impairment
Variation info
Gene OTOF
CLNDBN Hearing impairment
Reversed 1
HGVS NC_000002.11:g.26699187T>C
CLNSRC
CLNACC RCV000415433.1,