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rs1060499802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499802(C;T)
Make rs1060499802(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77211311
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1060499802
dbSNP (classic)rs1060499802
ClinGenrs1060499802
ebirs1060499802
HLIrs1060499802
Exacrs1060499802
Gnomadrs1060499802
Varsomers1060499802
LitVarrs1060499802
Maprs1060499802
PheGenIrs1060499802
Biobankrs1060499802
1000 genomesrs1060499802
hgdprs1060499802
ensemblrs1060499802
geneviewrs1060499802
scholarrs1060499802
googlers1060499802
pharmgkbrs1060499802
gwascentralrs1060499802
openSNPrs1060499802
23andMers1060499802
23andMe allrs1060499802
SNPshotrs1060499802
SNPdbers1060499802
MSV3drs1060499802
GWAS Ctlgrs1060499802
Max Magnitude0
ClinVar
Risk rs1060499802(T;T)
Alt rs1060499802(T;T)
Reference Rs1060499802(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76922356C>T
CLNSRC
CLNACC RCV000454181.1,