rs397516336

Orientation

plus

Stabilized

plus

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

Make rs397516336(-;-)

Make rs397516336(-;AT)

Reference

GRCh38 38.1/141

Chromosome

X

Position

83509177

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs397516336
dbSNP (classic)	rs397516336
ClinGen	rs397516336
ebi	rs397516336
HLI	rs397516336
Exac	rs397516336
Gnomad	rs397516336
Varsome	rs397516336
LitVar	rs397516336
Map	rs397516336
PheGenI	rs397516336
Biobank	rs397516336
1000 genomes	rs397516336
hgdp	rs397516336
ensembl	rs397516336
geneview	rs397516336
scholar	rs397516336
google	rs397516336
pharmgkb	rs397516336
gwascentral	rs397516336
openSNP	rs397516336
23andMe	rs397516336
SNPshot	rs397516336
SNPdbe	rs397516336
MSV3d	rs397516336
GWAS Ctlg	rs397516336

Max Magnitude

0

ClinVar
Risk	rs397516336(-;-)
Alt	rs397516336(-;-)
Reference	Rs397516336(AT;AT)
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.82764185_82764186delAT
CLNSRC	ClinVar
CLNACC	RCV000036260.2,