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rs727504639

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504639(-;-)
Make rs727504639(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26474623
GeneOTOF
is asnp
is mentioned by
dbSNPrs727504639
ebirs727504639
HLIrs727504639
Exacrs727504639
Varsomers727504639
Maprs727504639
PheGenIrs727504639
hapmaprs727504639
1000 genomesrs727504639
hgdprs727504639
ensemblrs727504639
gopubmedrs727504639
geneviewrs727504639
scholarrs727504639
googlers727504639
pharmgkbrs727504639
gwascentralrs727504639
openSNPrs727504639
23andMers727504639
23andMe allrs727504639
SNP Nexus

SNPshotrs727504639
SNPdbers727504639
MSV3drs727504639
GWAS Ctlgrs727504639
Max Magnitude0
ClinVar
Risk rs727504639(;)
Alt rs727504639(;)
Reference rs727504639(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26697491delC
CLNSRC
CLNACC RCV000155900.1,