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

rs727503316

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503316(A;A)
Make rs727503316(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position18151952
GeneLOC105371568, MYO15A
is asnp
is mentioned by
dbSNPrs727503316
ebirs727503316
HLIrs727503316
Exacrs727503316
Varsomers727503316
Maprs727503316
PheGenIrs727503316
hapmaprs727503316
1000 genomesrs727503316
hgdprs727503316
ensemblrs727503316
gopubmedrs727503316
geneviewrs727503316
scholarrs727503316
googlers727503316
pharmgkbrs727503316
gwascentralrs727503316
openSNPrs727503316
23andMers727503316
23andMe allrs727503316
SNP Nexus

SNPshotrs727503316
SNPdbers727503316
MSV3drs727503316
GWAS Ctlgrs727503316
Max Magnitude0
ClinVar
Risk rs727503316(A;A)
Alt rs727503316(A;A)
Reference rs727503316(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.18055266G>A
CLNSRC
CLNACC RCV000151411.1,