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rs768338261

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768338261(-;-)
Make rs768338261(-;TTC)
Make rs768338261(TTC;TTC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26470685
GeneOTOF
is asnp
is mentioned by
dbSNPrs768338261
ebirs768338261
HLIrs768338261
Exacrs768338261
Varsomers768338261
Maprs768338261
PheGenIrs768338261
hapmaprs768338261
1000 genomesrs768338261
hgdprs768338261
ensemblrs768338261
gopubmedrs768338261
geneviewrs768338261
scholarrs768338261
googlers768338261
pharmgkbrs768338261
gwascentralrs768338261
openSNPrs768338261
23andMers768338261
23andMe allrs768338261
SNP Nexus

SNPshotrs768338261
SNPdbers768338261
MSV3drs768338261
GWAS Ctlgrs768338261
Max Magnitude0
ClinVar
Risk rs768338261(CCTT,CCTTCTT;CCTT,CCTTCTT)
Alt rs768338261(CCTT,CCTTCTT;CCTT,CCTTCTT)
Reference rs768338261(C;C)
Significance Probable-Pathogenic
Disease Deafness not specified
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9 not specified
Reversed 0
HGVS NC_000002.11:g.26693554_26693556dupCTT
CLNSRC
CLNACC RCV000195955.1, RCV000214082.1,