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rs760980785

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760980785(A;A)
Make rs760980785(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18146035
GeneMYO15A
is asnp
is mentioned by
dbSNPrs760980785
ebirs760980785
HLIrs760980785
Exacrs760980785
Varsomers760980785
Maprs760980785
PheGenIrs760980785
hapmaprs760980785
1000 genomesrs760980785
hgdprs760980785
ensemblrs760980785
gopubmedrs760980785
geneviewrs760980785
scholarrs760980785
googlers760980785
pharmgkbrs760980785
gwascentralrs760980785
openSNPrs760980785
23andMers760980785
23andMe allrs760980785
SNP Nexus

SNPshotrs760980785
SNPdbers760980785
MSV3drs760980785
GWAS Ctlgrs760980785
Max Magnitude0
ClinVar
Risk rs760980785(A;A)
Alt rs760980785(A;A)
Reference rs760980785(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18049349G>A
CLNSRC
CLNACC RCV000215334.1,