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rs1057519606

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519606(C;C)
Make rs1057519606(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18159349
GeneMYO15A
is asnp
is mentioned by
dbSNPrs1057519606
dbSNP (old)rs1057519606
ClinGenrs1057519606
ebirs1057519606
HLIrs1057519606
Exacrs1057519606
Gnomadrs1057519606
Varsomers1057519606
Maprs1057519606
PheGenIrs1057519606
Biobankrs1057519606
1000 genomesrs1057519606
hgdprs1057519606
ensemblrs1057519606
gopubmedrs1057519606
geneviewrs1057519606
scholarrs1057519606
googlers1057519606
pharmgkbrs1057519606
gwascentralrs1057519606
openSNPrs1057519606
23andMers1057519606
23andMe allrs1057519606
SNPshotrs1057519606
SNPdbers1057519606
MSV3drs1057519606
GWAS Ctlgrs1057519606
Max Magnitude0
ClinVar
Risk rs1057519606(C;C)
Alt rs1057519606(C;C)
Reference Rs1057519606(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18062663T>C
CLNSRC
CLNACC RCV000417166.1,