Have questions? Visit https://www.reddit.com/r/SNPedia

rs199897298

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199897298(G;T)
Make rs199897298(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77184688
GeneMYO7A
is asnp
is mentioned by
dbSNPrs199897298
ebirs199897298
HLIrs199897298
Exacrs199897298
Varsomers199897298
Maprs199897298
PheGenIrs199897298
hapmaprs199897298
1000 genomesrs199897298
hgdprs199897298
ensemblrs199897298
gopubmedrs199897298
geneviewrs199897298
scholarrs199897298
googlers199897298
pharmgkbrs199897298
gwascentralrs199897298
openSNPrs199897298
23andMers199897298
23andMe allrs199897298
SNP Nexus

SNPshotrs199897298
SNPdbers199897298
MSV3drs199897298
GWAS Ctlgrs199897298
Max Magnitude0
ClinVar
Risk rs199897298(T;T)
Alt rs199897298(T;T)
Reference rs199897298(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76895733G>T
CLNSRC
CLNACC RCV000036110.3,