rs727505157

Merged into

rs397515597

Orientation

minus

Stabilized

minus

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

Make rs727505157(-;-)

Make rs727505157(-;AG)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

26475927

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs727505157
dbSNP (classic)	rs727505157
ClinGen	rs727505157
ebi	rs727505157
HLI	rs727505157
Exac	rs727505157
Gnomad	rs727505157
Varsome	rs727505157
LitVar	rs727505157
Map	rs727505157
PheGenI	rs727505157
Biobank	rs727505157
1000 genomes	rs727505157
hgdp	rs727505157
ensembl	rs727505157
geneview	rs727505157
scholar	rs727505157
google	rs727505157
pharmgkb	rs727505157
gwascentral	rs727505157
openSNP	rs727505157
23andMe	rs727505157
SNPshot	rs727505157
SNPdbe	rs727505157
MSV3d	rs727505157
GWAS Ctlg	rs727505157

Status

Merged into rs397515597

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs727505157(AG;AG)
Significance	Other
Disease	Deafness Non-syndromic genetic deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9 Non-syndromic genetic deafness
Reversed	1
HGVS	NC_000002.11:g.26698795_26698796delCT
CLNSRC
CLNACC	RCV000156627.2, RCV000211839.1,