rs398123070

Orientation

plus

Stabilized

plus

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

Make rs398123070(A;A)

Make rs398123070(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

146340404

Gene

POU4F3

is a	snp
is	mentioned by
dbSNP	rs398123070
dbSNP (classic)	rs398123070
ClinGen	rs398123070
ebi	rs398123070
HLI	rs398123070
Exac	rs398123070
Gnomad	rs398123070
Varsome	rs398123070
LitVar	rs398123070
Map	rs398123070
PheGenI	rs398123070
Biobank	rs398123070
1000 genomes	rs398123070
hgdp	rs398123070
ensembl	rs398123070
geneview	rs398123070
scholar	rs398123070
google	rs398123070
pharmgkb	rs398123070
gwascentral	rs398123070
openSNP	rs398123070
23andMe	rs398123070
SNPshot	rs398123070
SNPdbe	rs398123070
MSV3d	rs398123070
GWAS Ctlg	rs398123070

Max Magnitude

0

ClinVar
Risk	rs398123070(A;A)
Alt	rs398123070(A;A)
Reference	Rs398123070(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	POU4F3
CLNDBN	Deafness, autosomal dominant 15
Reversed	0
HGVS	NC_000005.9:g.145719967G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000082870.2,