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rs727503326

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503326(C;T)
Make rs727503326(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position75844906
GeneMYO6
is asnp
is mentioned by
dbSNPrs727503326
ebirs727503326
HLIrs727503326
Exacrs727503326
Varsomers727503326
Maprs727503326
PheGenIrs727503326
hapmaprs727503326
1000 genomesrs727503326
hgdprs727503326
ensemblrs727503326
gopubmedrs727503326
geneviewrs727503326
scholarrs727503326
googlers727503326
pharmgkbrs727503326
gwascentralrs727503326
openSNPrs727503326
23andMers727503326
23andMe allrs727503326
SNP Nexus

SNPshotrs727503326
SNPdbers727503326
MSV3drs727503326
GWAS Ctlgrs727503326
Max Magnitude0
ClinVar
Risk rs727503326(T;T)
Alt rs727503326(T;T)
Reference rs727503326(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO6
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000006.11:g.76554623C>T
CLNSRC
CLNACC RCV000151469.1,