rs1060499806

Orientation

plus

Stabilized

plus

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

Make rs1060499806(G;T)

Make rs1060499806(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

83509169

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs1060499806
dbSNP (classic)	rs1060499806
ClinGen	rs1060499806
ebi	rs1060499806
HLI	rs1060499806
Exac	rs1060499806
Gnomad	rs1060499806
Varsome	rs1060499806
LitVar	rs1060499806
Map	rs1060499806
PheGenI	rs1060499806
Biobank	rs1060499806
1000 genomes	rs1060499806
hgdp	rs1060499806
ensembl	rs1060499806
geneview	rs1060499806
scholar	rs1060499806
google	rs1060499806
pharmgkb	rs1060499806
gwascentral	rs1060499806
openSNP	rs1060499806
23andMe	rs1060499806
SNPshot	rs1060499806
SNPdbe	rs1060499806
MSV3d	rs1060499806
GWAS Ctlg	rs1060499806

Max Magnitude

0

ClinVar
Risk	rs1060499806(T;T)
Alt	rs1060499806(T;T)
Reference	Rs1060499806(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	POU3F4
CLNDBN	Deafness, X-linked 2
Reversed	0
HGVS	NC_000023.10:g.82764177G>T
CLNSRC
CLNACC	RCV000454255.1,