rs121918380

Orientation

minus

Stabilized

minus

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

Make rs121918380(C;T)

Make rs121918380(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

110263964

Gene

RDX

is a	snp
is	mentioned by
dbSNP	rs121918380
dbSNP (classic)	rs121918380
ClinGen	rs121918380
ebi	rs121918380
HLI	rs121918380
Exac	rs121918380
Gnomad	rs121918380
Varsome	rs121918380
LitVar	rs121918380
Map	rs121918380
PheGenI	rs121918380
Biobank	rs121918380
1000 genomes	rs121918380
hgdp	rs121918380
ensembl	rs121918380
geneview	rs121918380
scholar	rs121918380
google	rs121918380
pharmgkb	rs121918380
gwascentral	rs121918380
openSNP	rs121918380
23andMe	rs121918380
SNPshot	rs121918380
SNPdbe	rs121918380
MSV3d	rs121918380
GWAS Ctlg	rs121918380

Max Magnitude

0

OMIM	179410
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918380(T;T)
Alt	rs121918380(T;T)
Reference	Rs121918380(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	RDX
CLNDBN	Deafness, autosomal recessive 24
Reversed	1
HGVS	NC_000011.9:g.110134689G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014074.24,