rs104894920

Orientation

plus

Stabilized

plus

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

Make rs104894920(A;T)

Make rs104894920(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

83508928

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs104894920
dbSNP (classic)	rs104894920
ClinGen	rs104894920
ebi	rs104894920
HLI	rs104894920
Exac	rs104894920
Gnomad	rs104894920
Varsome	rs104894920
LitVar	rs104894920
Map	rs104894920
PheGenI	rs104894920
Biobank	rs104894920
1000 genomes	rs104894920
hgdp	rs104894920
ensembl	rs104894920
geneview	rs104894920
scholar	rs104894920
google	rs104894920
pharmgkb	rs104894920
gwascentral	rs104894920
openSNP	rs104894920
23andMe	rs104894920
SNPshot	rs104894920
SNPdbe	rs104894920
MSV3d	rs104894920
GWAS Ctlg	rs104894920

Max Magnitude

0

OMIM	300039
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104894920(T;T)
Alt	rs104894920(T;T)
Reference	Rs104894920(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	POU3F4
CLNDBN	Deafness, X-linked 2
Reversed	0
HGVS	NC_000023.10:g.82763936A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012444.15,