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rs797045088

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045088(A;A)
Make rs797045088(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position133525153
GeneEYA4, TARID
is asnp
is mentioned by
dbSNPrs797045088
ebirs797045088
HLIrs797045088
Exacrs797045088
Varsomers797045088
Maprs797045088
PheGenIrs797045088
hapmaprs797045088
1000 genomesrs797045088
hgdprs797045088
ensemblrs797045088
gopubmedrs797045088
geneviewrs797045088
scholarrs797045088
googlers797045088
pharmgkbrs797045088
gwascentralrs797045088
openSNPrs797045088
23andMers797045088
23andMe allrs797045088
SNP Nexus

SNPshotrs797045088
SNPdbers797045088
MSV3drs797045088
GWAS Ctlgrs797045088
Max Magnitude0
ClinVar
Risk rs797045088(A;A)
Alt rs797045088(A;A)
Reference rs797045088(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene EYA4 TARID
CLNDBN Deafness, autosomal dominant 10
Reversed 0
HGVS NC_000006.11:g.133846291G>A
CLNSRC
CLNACC RCV000190582.1,