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rs201539845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201539845(A;A)
Make rs201539845(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77156921
GeneMYO7A
is asnp
is mentioned by
dbSNPrs201539845
ebirs201539845
HLIrs201539845
Exacrs201539845
Varsomers201539845
Maprs201539845
PheGenIrs201539845
hapmaprs201539845
1000 genomesrs201539845
hgdprs201539845
ensemblrs201539845
gopubmedrs201539845
geneviewrs201539845
scholarrs201539845
googlers201539845
pharmgkbrs201539845
gwascentralrs201539845
openSNPrs201539845
23andMers201539845
23andMe allrs201539845
SNP Nexus

SNPshotrs201539845
SNPdbers201539845
MSV3drs201539845
GWAS Ctlgrs201539845
Max Magnitude0
ClinVar
Risk rs201539845(A;A)
Alt rs201539845(A;A)
Reference rs201539845(G;G)
Significance Pathogenic
Disease Deafness Usher syndrome
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal dominant 11 Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76867967G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022815.15, RCV000215956.1,