rs727504709

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs727504709(-;-)

Make rs727504709(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

110236135

Gene

RDX

is a	snp
is	mentioned by
dbSNP	rs727504709
dbSNP (classic)	rs727504709
ClinGen	rs727504709
ebi	rs727504709
HLI	rs727504709
Exac	rs727504709
Gnomad	rs727504709
Varsome	rs727504709
LitVar	rs727504709
Map	rs727504709
PheGenI	rs727504709
Biobank	rs727504709
1000 genomes	rs727504709
hgdp	rs727504709
ensembl	rs727504709
geneview	rs727504709
scholar	rs727504709
google	rs727504709
pharmgkb	rs727504709
gwascentral	rs727504709
openSNP	rs727504709
23andMe	rs727504709
SNPshot	rs727504709
SNPdbe	rs727504709
MSV3d	rs727504709
GWAS Ctlg	rs727504709

Max Magnitude

0

ClinVar
Risk	rs727504709(-;-)
Alt	rs727504709(-;-)
Reference	Rs727504709(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	RDX
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000011.9:g.110106860delC
CLNSRC
CLNACC	RCV000155993.1,