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rs377670513

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377670513(C;T)
Make rs377670513(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77211909
GeneMYO7A
is asnp
is mentioned by
dbSNPrs377670513
ebirs377670513
HLIrs377670513
Exacrs377670513
Varsomers377670513
Maprs377670513
PheGenIrs377670513
hapmaprs377670513
1000 genomesrs377670513
hgdprs377670513
ensemblrs377670513
gopubmedrs377670513
geneviewrs377670513
scholarrs377670513
googlers377670513
pharmgkbrs377670513
gwascentralrs377670513
openSNPrs377670513
23andMers377670513
23andMe allrs377670513
SNP Nexus

SNPshotrs377670513
SNPdbers377670513
MSV3drs377670513
GWAS Ctlgrs377670513
Max Magnitude0
ClinVar
Risk rs377670513(T;T)
Alt rs377670513(T;T)
Reference rs377670513(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76922954C>T
CLNSRC
CLNACC RCV000151522.2,