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rs727505157

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs727505157(-;-)
Make rs727505157(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26475927
GeneOTOF
is asnp
is mentioned by
dbSNPrs727505157
ebirs727505157
HLIrs727505157
Exacrs727505157
Varsomers727505157
Maprs727505157
PheGenIrs727505157
hapmaprs727505157
1000 genomesrs727505157
hgdprs727505157
ensemblrs727505157
gopubmedrs727505157
geneviewrs727505157
scholarrs727505157
googlers727505157
pharmgkbrs727505157
gwascentralrs727505157
openSNPrs727505157
23andMers727505157
23andMe allrs727505157
SNP Nexus

SNPshotrs727505157
SNPdbers727505157
MSV3drs727505157
GWAS Ctlgrs727505157
Max Magnitude0
ClinVar
Risk rs727505157(;)
Alt rs727505157(;)
Reference rs727505157(AG;AG)
Significance Other
Disease Deafness Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9 Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26698795_26698796delCT
CLNSRC
CLNACC RCV000156627.2, RCV000211839.1,