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

rs606231379

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231379(-;-)
Make rs606231379(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77162854
GeneMYO7A
is asnp
is mentioned by
dbSNPrs606231379
ebirs606231379
HLIrs606231379
Exacrs606231379
Varsomers606231379
Maprs606231379
PheGenIrs606231379
hapmaprs606231379
1000 genomesrs606231379
hgdprs606231379
ensemblrs606231379
gopubmedrs606231379
geneviewrs606231379
scholarrs606231379
googlers606231379
pharmgkbrs606231379
gwascentralrs606231379
openSNPrs606231379
23andMers606231379
23andMe allrs606231379
SNP Nexus

SNPshotrs606231379
SNPdbers606231379
MSV3drs606231379
GWAS Ctlgrs606231379
Max Magnitude0
ClinVar
Risk rs606231379(;)
Alt rs606231379(;)
Reference rs606231379(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76873900delG
CLNSRC
CLNACC RCV000036056.2,