rs727504639

Orientation

minus

Stabilized

minus

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

Make rs727504639(-;-)

Make rs727504639(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

26474623

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs727504639
dbSNP (classic)	rs727504639
ClinGen	rs727504639
ebi	rs727504639
HLI	rs727504639
Exac	rs727504639
Gnomad	rs727504639
Varsome	rs727504639
LitVar	rs727504639
Map	rs727504639
PheGenI	rs727504639
Biobank	rs727504639
1000 genomes	rs727504639
hgdp	rs727504639
ensembl	rs727504639
geneview	rs727504639
scholar	rs727504639
google	rs727504639
pharmgkb	rs727504639
gwascentral	rs727504639
openSNP	rs727504639
23andMe	rs727504639
SNPshot	rs727504639
SNPdbe	rs727504639
MSV3d	rs727504639
GWAS Ctlg	rs727504639

Max Magnitude

0

ClinVar
Risk	rs727504639(-;-)
Alt	rs727504639(-;-)
Reference	Rs727504639(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOF
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000002.11:g.26697491delC
CLNSRC
CLNACC	RCV000155900.1,