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rs1060499801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499801(C;T)
Make rs1060499801(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77211296
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1060499801
dbSNP (classic)rs1060499801
ClinGenrs1060499801
ebirs1060499801
HLIrs1060499801
Exacrs1060499801
Gnomadrs1060499801
Varsomers1060499801
LitVarrs1060499801
Maprs1060499801
PheGenIrs1060499801
Biobankrs1060499801
1000 genomesrs1060499801
hgdprs1060499801
ensemblrs1060499801
geneviewrs1060499801
scholarrs1060499801
googlers1060499801
pharmgkbrs1060499801
gwascentralrs1060499801
openSNPrs1060499801
23andMers1060499801
23andMe allrs1060499801
SNPshotrs1060499801
SNPdbers1060499801
MSV3drs1060499801
GWAS Ctlgrs1060499801
Max Magnitude0
ClinVar
Risk rs1060499801(T;T)
Alt rs1060499801(T;T)
Reference Rs1060499801(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76922341C>T
CLNSRC
CLNACC RCV000454216.1,