rs876657719

Orientation

plus

Stabilized

plus

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

Make rs876657719(-;-)

Make rs876657719(-;CAAA)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

83508931

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs876657719
dbSNP (classic)	rs876657719
ClinGen	rs876657719
ebi	rs876657719
HLI	rs876657719
Exac	rs876657719
Gnomad	rs876657719
Varsome	rs876657719
LitVar	rs876657719
Map	rs876657719
PheGenI	rs876657719
Biobank	rs876657719
1000 genomes	rs876657719
hgdp	rs876657719
ensembl	rs876657719
geneview	rs876657719
scholar	rs876657719
google	rs876657719
pharmgkb	rs876657719
gwascentral	rs876657719
openSNP	rs876657719
23andMe	rs876657719
SNPshot	rs876657719
SNPdbe	rs876657719
MSV3d	rs876657719
GWAS Ctlg	rs876657719

Max Magnitude

0

ClinVar
Risk	rs876657719(-;-)
Alt	rs876657719(-;-)
Reference	Rs876657719(CAAA;CAAA)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	POU3F4
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000023.10:g.82763939_82763942delCAAA
CLNSRC
CLNACC	RCV000215388.1,