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rs797044490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCAT;CCAT) 0 common in clinvar
Make rs797044490(-;-)
Make rs797044490(-;ATCC)
Make rs797044490(ATCC;ATCC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77158400
GeneMYO7A
is asnp
is mentioned by
dbSNPrs797044490
dbSNP (old)rs797044490
ClinGenrs797044490
ebirs797044490
HLIrs797044490
Exacrs797044490
Gnomadrs797044490
Varsomers797044490
Maprs797044490
PheGenIrs797044490
Biobankrs797044490
1000 genomesrs797044490
hgdprs797044490
ensemblrs797044490
gopubmedrs797044490
geneviewrs797044490
scholarrs797044490
googlers797044490
pharmgkbrs797044490
gwascentralrs797044490
openSNPrs797044490
23andMers797044490
23andMe allrs797044490
SNP Nexus

SNPshotrs797044490
SNPdbers797044490
MSV3drs797044490
GWAS Ctlgrs797044490
Max Magnitude0
ClinVar
Risk rs797044490(-;-)
Alt rs797044490(-;-)
Reference Rs797044490(CCAT;CCAT)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76869446_76869449delATCC
CLNSRC
CLNACC RCV000151481.1,