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

rs727503284

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503284(G;T)
Make rs727503284(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position36289096
GeneMYH9
is asnp
is mentioned by
dbSNPrs727503284
ebirs727503284
HLIrs727503284
Exacrs727503284
Varsomers727503284
Maprs727503284
PheGenIrs727503284
hapmaprs727503284
1000 genomesrs727503284
hgdprs727503284
ensemblrs727503284
gopubmedrs727503284
geneviewrs727503284
scholarrs727503284
googlers727503284
pharmgkbrs727503284
gwascentralrs727503284
openSNPrs727503284
23andMers727503284
23andMe allrs727503284
SNP Nexus

SNPshotrs727503284
SNPdbers727503284
MSV3drs727503284
GWAS Ctlgrs727503284
Max Magnitude0
ClinVar
Risk rs727503284(T;T)
Alt rs727503284(T;T)
Reference rs727503284(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYH9
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000022.10:g.36685142C>A
CLNSRC
CLNACC RCV000151326.1,