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rs376764423

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376764423(C;T)
Make rs376764423(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77208472
GeneMYO7A
is asnp
is mentioned by
dbSNPrs376764423
ebirs376764423
HLIrs376764423
Exacrs376764423
Varsomers376764423
Maprs376764423
PheGenIrs376764423
hapmaprs376764423
1000 genomesrs376764423
hgdprs376764423
ensemblrs376764423
gopubmedrs376764423
geneviewrs376764423
scholarrs376764423
googlers376764423
pharmgkbrs376764423
gwascentralrs376764423
openSNPrs376764423
23andMers376764423
23andMe allrs376764423
SNP Nexus

SNPshotrs376764423
SNPdbers376764423
MSV3drs376764423
GWAS Ctlgrs376764423
Max Magnitude0
ClinVar
Risk rs376764423(T;T)
Alt rs376764423(T;T)
Reference rs376764423(C;C)
Significance Pathogenic
Disease Usher syndrome Retinal dystrophy
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1 Retinal dystrophy
Reversed 0
HGVS NC_000011.9:g.76919517C>T
CLNSRC
CLNACC RCV000155243.1, RCV000225571.1,