rs104894922

Orientation

plus

Stabilized

plus

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

Make rs104894922(A;G)

Make rs104894922(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

83509324

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs104894922
dbSNP (classic)	rs104894922
ClinGen	rs104894922
ebi	rs104894922
HLI	rs104894922
Exac	rs104894922
Gnomad	rs104894922
Varsome	rs104894922
LitVar	rs104894922
Map	rs104894922
PheGenI	rs104894922
Biobank	rs104894922
1000 genomes	rs104894922
hgdp	rs104894922
ensembl	rs104894922
geneview	rs104894922
scholar	rs104894922
google	rs104894922
pharmgkb	rs104894922
gwascentral	rs104894922
openSNP	rs104894922
23andMe	rs104894922
SNPshot	rs104894922
SNPdbe	rs104894922
MSV3d	rs104894922
GWAS Ctlg	rs104894922

Max Magnitude

0

OMIM	300039
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894922(G;G)
Alt	rs104894922(G;G)
Reference	Rs104894922(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	POU3F4
CLNDBN	Deafness, X-linked 2
Reversed	0
HGVS	NC_000023.10:g.82764332A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012446.25,