rs727503528

Orientation

plus

Stabilized

plus

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

Make rs727503528(C;T)

Make rs727503528(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

37769050

Gene

TRIOBP

is a	snp
is	mentioned by
dbSNP	rs727503528
dbSNP (classic)	rs727503528
ClinGen	rs727503528
ebi	rs727503528
HLI	rs727503528
Exac	rs727503528
Gnomad	rs727503528
Varsome	rs727503528
LitVar	rs727503528
Map	rs727503528
PheGenI	rs727503528
Biobank	rs727503528
1000 genomes	rs727503528
hgdp	rs727503528
ensembl	rs727503528
geneview	rs727503528
scholar	rs727503528
google	rs727503528
pharmgkb	rs727503528
gwascentral	rs727503528
openSNP	rs727503528
23andMe	rs727503528
SNPshot	rs727503528
SNPdbe	rs727503528
MSV3d	rs727503528
GWAS Ctlg	rs727503528

Max Magnitude

0

ClinVar
Risk	rs727503528(T;T)
Alt	rs727503528(T;T)
Reference	Rs727503528(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	TRIOBP
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000022.10:g.38165057C>T
CLNSRC
CLNACC	RCV000152152.1,