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rs191710555

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs191710555(C;T)
Make rs191710555(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18120023
GeneLOC105371566, MYO15A
is asnp
is mentioned by
dbSNPrs191710555
dbSNP (old)rs191710555
ClinGenrs191710555
ebirs191710555
HLIrs191710555
Exacrs191710555
Gnomadrs191710555
Varsomers191710555
Maprs191710555
PheGenIrs191710555
Biobankrs191710555
1000 genomesrs191710555
hgdprs191710555
ensemblrs191710555
gopubmedrs191710555
geneviewrs191710555
scholarrs191710555
googlers191710555
pharmgkbrs191710555
gwascentralrs191710555
openSNPrs191710555
23andMers191710555
23andMe allrs191710555
SNPshotrs191710555
SNPdbers191710555
MSV3drs191710555
GWAS Ctlgrs191710555
Max Magnitude0
ClinVar
Risk rs191710555(T;T)
Alt rs191710555(T;T)
Reference Rs191710555(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18023337C>T
CLNSRC
CLNACC RCV000454352.1,