Rs121908929

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908929(C;C)
Make rs121908929(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position30878920
GeneCOCH, RPS4XP13
is asnp
is mentioned by
dbSNPrs121908929
Exacrs121908929
PheGenIrs121908929
nextbiors121908929
hapmaprs121908929
1000 genomesrs121908929
hgdprs121908929
ensemblrs121908929
gopubmedrs121908929
geneviewrs121908929
scholarrs121908929
googlers121908929
pharmgkbrs121908929
gwascentralrs121908929
openSNPrs121908929
23andMers121908929
23andMe allrs121908929
SNP Nexus

SNPshotrs121908929
SNPdbers121908929
MSV3drs121908929
Max Magnitude0
OMIM603196
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908929(C;C)
Alt rs121908929(C;C)
Reference rs121908929(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene RP11-829H16.3 COCH
CLNDBN Deafness, autosomal dominant 9
Reversed 0
HGVS NC_000014.8:g.31348126T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006989.2,