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rs369458838

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369458838(C;T)
Make rs369458838(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77190773
GeneMYO7A
is asnp
is mentioned by
dbSNPrs369458838
ClinGenrs369458838
ebirs369458838
HLIrs369458838
Exacrs369458838
Varsomers369458838
Maprs369458838
PheGenIrs369458838
hapmaprs369458838
1000 genomesrs369458838
hgdprs369458838
ensemblrs369458838
gopubmedrs369458838
geneviewrs369458838
scholarrs369458838
googlers369458838
pharmgkbrs369458838
gwascentralrs369458838
openSNPrs369458838
23andMers369458838
23andMe allrs369458838
SNP Nexus

SNPshotrs369458838
SNPdbers369458838
MSV3drs369458838
GWAS Ctlgrs369458838
Max Magnitude0
ClinVar
Risk rs369458838(T;T)
Alt rs369458838(T;T)
Reference Rs369458838(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76901818C>T
CLNSRC
CLNACC RCV000155024.1,