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rs727503309

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503309(A;A)
Make rs727503309(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position18141144
GeneMYO15A
is asnp
is mentioned by
dbSNPrs727503309
ebirs727503309
HLIrs727503309
Exacrs727503309
Varsomers727503309
Maprs727503309
PheGenIrs727503309
hapmaprs727503309
1000 genomesrs727503309
hgdprs727503309
ensemblrs727503309
gopubmedrs727503309
geneviewrs727503309
scholarrs727503309
googlers727503309
pharmgkbrs727503309
gwascentralrs727503309
openSNPrs727503309
23andMers727503309
23andMe allrs727503309
SNP Nexus

SNPshotrs727503309
SNPdbers727503309
MSV3drs727503309
GWAS Ctlgrs727503309
Max Magnitude0
ClinVar
Risk rs727503309(A;A)
Alt rs727503309(A;A)
Reference rs727503309(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18044458G>A
CLNSRC
CLNACC RCV000151394.1,