Have questions? Visit https://www.reddit.com/r/SNPedia

rs727505359

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505359(-;-)
Make rs727505359(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26458109
GeneOTOF
is asnp
is mentioned by
dbSNPrs727505359
ebirs727505359
HLIrs727505359
Exacrs727505359
Varsomers727505359
Maprs727505359
PheGenIrs727505359
hapmaprs727505359
1000 genomesrs727505359
hgdprs727505359
ensemblrs727505359
gopubmedrs727505359
geneviewrs727505359
scholarrs727505359
googlers727505359
pharmgkbrs727505359
gwascentralrs727505359
openSNPrs727505359
23andMers727505359
23andMe allrs727505359
SNP Nexus

SNPshotrs727505359
SNPdbers727505359
MSV3drs727505359
GWAS Ctlgrs727505359
Max Magnitude0
ClinVar
Risk rs727505359(;)
Alt rs727505359(;)
Reference rs727505359(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26680977delC
CLNSRC
CLNACC RCV000156924.1,