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rs1060499803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499803(A;G)
Make rs1060499803(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77194352
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1060499803
dbSNP (old)rs1060499803
ClinGenrs1060499803
ebirs1060499803
HLIrs1060499803
Exacrs1060499803
Gnomadrs1060499803
Varsomers1060499803
LitVarrs1060499803
Maprs1060499803
PheGenIrs1060499803
Biobankrs1060499803
1000 genomesrs1060499803
hgdprs1060499803
ensemblrs1060499803
gopubmedrs1060499803
geneviewrs1060499803
scholarrs1060499803
googlers1060499803
pharmgkbrs1060499803
gwascentralrs1060499803
openSNPrs1060499803
23andMers1060499803
23andMe allrs1060499803
SNPshotrs1060499803
SNPdbers1060499803
MSV3drs1060499803
GWAS Ctlgrs1060499803
Max Magnitude0
ClinVar
Risk rs1060499803(G;G)
Alt rs1060499803(G;G)
Reference Rs1060499803(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76905397A>G
CLNSRC
CLNACC RCV000454153.1,