Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519603(C;C)
Make rs1057519603(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18126856
GeneMYO15A
is asnp
is mentioned by
dbSNPrs1057519603
dbSNP (classic)rs1057519603
ClinGenrs1057519603
ebirs1057519603
HLIrs1057519603
Exacrs1057519603
Gnomadrs1057519603
Varsomers1057519603
LitVarrs1057519603
Maprs1057519603
PheGenIrs1057519603
Biobankrs1057519603
1000 genomesrs1057519603
hgdprs1057519603
ensemblrs1057519603
geneviewrs1057519603
scholarrs1057519603
googlers1057519603
pharmgkbrs1057519603
gwascentralrs1057519603
openSNPrs1057519603
23andMers1057519603
23andMe allrs1057519603
SNPshotrs1057519603
SNPdbers1057519603
MSV3drs1057519603
GWAS Ctlgrs1057519603
Max Magnitude0
ClinVar
Risk rs1057519603(C;C)
Alt rs1057519603(C;C)
Reference Rs1057519603(T;T)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18030170T>C
CLNSRC
CLNACC RCV000417169.1,