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rs1060499800

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499800(-;-)
Make rs1060499800(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77179069
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1060499800
dbSNP (old)rs1060499800
ClinGenrs1060499800
ebirs1060499800
HLIrs1060499800
Exacrs1060499800
Gnomadrs1060499800
Varsomers1060499800
LitVarrs1060499800
Maprs1060499800
PheGenIrs1060499800
Biobankrs1060499800
1000 genomesrs1060499800
hgdprs1060499800
ensemblrs1060499800
gopubmedrs1060499800
geneviewrs1060499800
scholarrs1060499800
googlers1060499800
pharmgkbrs1060499800
gwascentralrs1060499800
openSNPrs1060499800
23andMers1060499800
23andMe allrs1060499800
SNPshotrs1060499800
SNPdbers1060499800
MSV3drs1060499800
GWAS Ctlgrs1060499800
Max Magnitude0
ClinVar
Risk rs1060499800(-;-)
Alt rs1060499800(-;-)
Reference Rs1060499800(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76890115delC
CLNSRC
CLNACC RCV000454349.1,