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rs727504936

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504936(C;T)
Make rs727504936(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26476176
GeneOTOF
is asnp
is mentioned by
dbSNPrs727504936
ebirs727504936
HLIrs727504936
Exacrs727504936
Varsomers727504936
Maprs727504936
PheGenIrs727504936
hapmaprs727504936
1000 genomesrs727504936
hgdprs727504936
ensemblrs727504936
gopubmedrs727504936
geneviewrs727504936
scholarrs727504936
googlers727504936
pharmgkbrs727504936
gwascentralrs727504936
openSNPrs727504936
23andMers727504936
23andMe allrs727504936
SNP Nexus

SNPshotrs727504936
SNPdbers727504936
MSV3drs727504936
GWAS Ctlgrs727504936
Max Magnitude0
ClinVar
Risk rs727504936(T;T)
Alt rs727504936(T;T)
Reference rs727504936(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26699044G>A
CLNSRC
CLNACC RCV000156331.1,