rs876657643

Orientation

plus

Stabilized

plus

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

Make rs876657643(-;-)

Make rs876657643(-;TG)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

76491684

Gene

ESRRB

is a	snp
is	mentioned by
dbSNP	rs876657643
dbSNP (classic)	rs876657643
ClinGen	rs876657643
ebi	rs876657643
HLI	rs876657643
Exac	rs876657643
Gnomad	rs876657643
Varsome	rs876657643
LitVar	rs876657643
Map	rs876657643
PheGenI	rs876657643
Biobank	rs876657643
1000 genomes	rs876657643
hgdp	rs876657643
ensembl	rs876657643
geneview	rs876657643
scholar	rs876657643
google	rs876657643
pharmgkb	rs876657643
gwascentral	rs876657643
openSNP	rs876657643
23andMe	rs876657643
SNPshot	rs876657643
SNPdbe	rs876657643
MSV3d	rs876657643
GWAS Ctlg	rs876657643

Max Magnitude

0

ClinVar
Risk	rs876657643(-;-)
Alt	rs876657643(-;-)
Reference	Rs876657643(TG;TG)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	ESRRB
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000014.8:g.76958027_76958028delTG
CLNSRC
CLNACC	RCV000218592.1,