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rs727503329

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503329(A;A)
Make rs727503329(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77190838
GeneMYO7A
is asnp
is mentioned by
dbSNPrs727503329
ebirs727503329
HLIrs727503329
Exacrs727503329
Varsomers727503329
Maprs727503329
PheGenIrs727503329
hapmaprs727503329
1000 genomesrs727503329
hgdprs727503329
ensemblrs727503329
gopubmedrs727503329
geneviewrs727503329
scholarrs727503329
googlers727503329
pharmgkbrs727503329
gwascentralrs727503329
openSNPrs727503329
23andMers727503329
23andMe allrs727503329
SNP Nexus

SNPshotrs727503329
SNPdbers727503329
MSV3drs727503329
GWAS Ctlgrs727503329
Max Magnitude0
ClinVar
Risk rs727503329(A;A)
Alt rs727503329(A;A)
Reference rs727503329(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76901883G>A
CLNSRC
CLNACC RCV000151505.2,