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rs727504541

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504541(A;C)
Make rs727504541(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77204213
GeneMYO7A
is asnp
is mentioned by
dbSNPrs727504541
ebirs727504541
HLIrs727504541
Exacrs727504541
Varsomers727504541
Maprs727504541
PheGenIrs727504541
hapmaprs727504541
1000 genomesrs727504541
hgdprs727504541
ensemblrs727504541
gopubmedrs727504541
geneviewrs727504541
scholarrs727504541
googlers727504541
pharmgkbrs727504541
gwascentralrs727504541
openSNPrs727504541
23andMers727504541
23andMe allrs727504541
SNP Nexus

SNPshotrs727504541
SNPdbers727504541
MSV3drs727504541
GWAS Ctlgrs727504541
Max Magnitude0
ClinVar
Risk rs727504541(C;C)
Alt rs727504541(C;C)
Reference rs727504541(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76915258A>C
CLNSRC
CLNACC RCV000155694.1,