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rs727504709

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504709(-;-)
Make rs727504709(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position110236135
GeneRDX
is asnp
is mentioned by
dbSNPrs727504709
ebirs727504709
HLIrs727504709
Exacrs727504709
Varsomers727504709
Maprs727504709
PheGenIrs727504709
hapmaprs727504709
1000 genomesrs727504709
hgdprs727504709
ensemblrs727504709
gopubmedrs727504709
geneviewrs727504709
scholarrs727504709
googlers727504709
pharmgkbrs727504709
gwascentralrs727504709
openSNPrs727504709
23andMers727504709
23andMe allrs727504709
SNP Nexus

SNPshotrs727504709
SNPdbers727504709
MSV3drs727504709
GWAS Ctlgrs727504709
Max Magnitude0
ClinVar
Risk rs727504709(;)
Alt rs727504709(;)
Reference rs727504709(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene RDX
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000011.9:g.110106860delC
CLNSRC
CLNACC RCV000155993.1,