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rs727504567

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504567(C;T)
Make rs727504567(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position75828590
GeneMYO6
is asnp
is mentioned by
dbSNPrs727504567
ebirs727504567
HLIrs727504567
Exacrs727504567
Varsomers727504567
Maprs727504567
PheGenIrs727504567
hapmaprs727504567
1000 genomesrs727504567
hgdprs727504567
ensemblrs727504567
gopubmedrs727504567
geneviewrs727504567
scholarrs727504567
googlers727504567
pharmgkbrs727504567
gwascentralrs727504567
openSNPrs727504567
23andMers727504567
23andMe allrs727504567
SNP Nexus

SNPshotrs727504567
SNPdbers727504567
MSV3drs727504567
GWAS Ctlgrs727504567
Max Magnitude0
ClinVar
Risk rs727504567(T;T)
Alt rs727504567(T;T)
Reference rs727504567(C;C)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO6
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000006.11:g.76538307C>T
CLNSRC
CLNACC RCV000155733.1,