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rs730880367

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880367(-;-)
Make rs730880367(-;G)
Make rs730880367(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77211331
GeneMYO7A
is asnp
is mentioned by
dbSNPrs730880367
ebirs730880367
HLIrs730880367
Exacrs730880367
Varsomers730880367
Maprs730880367
PheGenIrs730880367
hapmaprs730880367
1000 genomesrs730880367
hgdprs730880367
ensemblrs730880367
gopubmedrs730880367
geneviewrs730880367
scholarrs730880367
googlers730880367
pharmgkbrs730880367
gwascentralrs730880367
openSNPrs730880367
23andMers730880367
23andMe allrs730880367
SNP Nexus

SNPshotrs730880367
SNPdbers730880367
MSV3drs730880367
GWAS Ctlgrs730880367
Max Magnitude0
ClinVar
Risk rs730880367(G;G)
Alt rs730880367(G;G)
Reference rs730880367(;)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76922376dupG
CLNSRC
CLNACC RCV000156543.1,