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rs797044564

From SNPedia

Orientationplus
Make rs797044564(-;-)
Make rs797044564(-;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77189426
GeneMYO7A
is asnp
is mentioned by
dbSNPrs797044564
ebirs797044564
HLIrs797044564
Exacrs797044564
Varsomers797044564
Maprs797044564
PheGenIrs797044564
hapmaprs797044564
1000 genomesrs797044564
hgdprs797044564
ensemblrs797044564
gopubmedrs797044564
geneviewrs797044564
scholarrs797044564
googlers797044564
pharmgkbrs797044564
gwascentralrs797044564
openSNPrs797044564
23andMers797044564
23andMe allrs797044564
SNP Nexus

SNPshotrs797044564
SNPdbers797044564
MSV3drs797044564
GWAS Ctlgrs797044564
Max Magnitude
ClinVar
Risk rs797044564(;)
Alt rs797044564(;)
Reference rs797044564(TC;TC)
Significance Pathogenic
Disease not provided Usher syndrome
Variation info
Gene MYO7A
CLNDBN not provided Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76900476_76900477delCT
CLNSRC
CLNACC RCV000171464.1, RCV000222358.1,