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rs139889944

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139889944(A;A)
Make rs139889944(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77199771
GeneMYO7A
is asnp
is mentioned by
dbSNPrs139889944
ebirs139889944
HLIrs139889944
Exacrs139889944
Varsomers139889944
Maprs139889944
PheGenIrs139889944
hapmaprs139889944
1000 genomesrs139889944
hgdprs139889944
ensemblrs139889944
gopubmedrs139889944
geneviewrs139889944
scholarrs139889944
googlers139889944
pharmgkbrs139889944
gwascentralrs139889944
openSNPrs139889944
23andMers139889944
23andMe allrs139889944
SNP Nexus

SNPshotrs139889944
SNPdbers139889944
MSV3drs139889944
GWAS Ctlgrs139889944
Max Magnitude0
ClinVar
Risk rs139889944(A;A)
Alt rs139889944(A;A)
Reference rs139889944(G;G)
Significance Pathogenic
Disease not specified not provided Usher syndrome
Variation info
Gene MYO7A
CLNDBN not specified not provided Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76910816G>A
CLNSRC
CLNACC RCV000036165.3, RCV000132572.1, RCV000223626.1,