rs727505246

Orientation

plus

Stabilized

plus

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

Make rs727505246(A;A)

Make rs727505246(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

83509292

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs727505246
dbSNP (classic)	rs727505246
ClinGen	rs727505246
ebi	rs727505246
HLI	rs727505246
Exac	rs727505246
Gnomad	rs727505246
Varsome	rs727505246
LitVar	rs727505246
Map	rs727505246
PheGenI	rs727505246
Biobank	rs727505246
1000 genomes	rs727505246
hgdp	rs727505246
ensembl	rs727505246
geneview	rs727505246
scholar	rs727505246
google	rs727505246
pharmgkb	rs727505246
gwascentral	rs727505246
openSNP	rs727505246
23andMe	rs727505246
SNPshot	rs727505246
SNPdbe	rs727505246
MSV3d	rs727505246
GWAS Ctlg	rs727505246

Max Magnitude

0

ClinVar
Risk	rs727505246(A;A)
Alt	rs727505246(A;A)
Reference	Rs727505246(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	POU3F4
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000023.10:g.82764300G>A
CLNSRC
CLNACC	RCV000156766.2,