rs876657644

Orientation

plus

Stabilized

plus

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

Make rs876657644(A;C)

Make rs876657644(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

133461112

Gene	EYA4, LOC107984121

is a	snp
is	mentioned by
dbSNP	rs876657644
dbSNP (classic)	rs876657644
ClinGen	rs876657644
ebi	rs876657644
HLI	rs876657644
Exac	rs876657644
Gnomad	rs876657644
Varsome	rs876657644
LitVar	rs876657644
Map	rs876657644
PheGenI	rs876657644
Biobank	rs876657644
1000 genomes	rs876657644
hgdp	rs876657644
ensembl	rs876657644
geneview	rs876657644
scholar	rs876657644
google	rs876657644
pharmgkb	rs876657644
gwascentral	rs876657644
openSNP	rs876657644
23andMe	rs876657644
SNPshot	rs876657644
SNPdbe	rs876657644
MSV3d	rs876657644
GWAS Ctlg	rs876657644

Max Magnitude

0

ClinVar
Risk	rs876657644(C;C)
Alt	rs876657644(C;C)
Reference	Rs876657644(A;A)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	EYA4 LOC101928164
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000006.11:g.133782250A>C
CLNSRC
CLNACC	RCV000223505.1,