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rs397516304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516304(-;-)
Make rs397516304(-;C)
Make rs397516304(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77190117
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516304
ebirs397516304
HLIrs397516304
Exacrs397516304
Varsomers397516304
Maprs397516304
PheGenIrs397516304
hapmaprs397516304
1000 genomesrs397516304
hgdprs397516304
ensemblrs397516304
gopubmedrs397516304
geneviewrs397516304
scholarrs397516304
googlers397516304
pharmgkbrs397516304
gwascentralrs397516304
openSNPrs397516304
23andMers397516304
23andMe allrs397516304
SNP Nexus

SNPshotrs397516304
SNPdbers397516304
MSV3drs397516304
GWAS Ctlgrs397516304
Max Magnitude0
ClinVar
Risk rs397516304(C;C)
Alt rs397516304(C;C)
Reference rs397516304(;)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76901162dupC
CLNSRC ClinVar
CLNACC RCV000036123.2,