rs549095193

Orientation

plus

Stabilized

plus

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

Make rs549095193(A;A)

Make rs549095193(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

37725611

Gene

TRIOBP

is a	snp
is	mentioned by
dbSNP	rs549095193
dbSNP (classic)	rs549095193
ClinGen	rs549095193
ebi	rs549095193
HLI	rs549095193
Exac	rs549095193
Gnomad	rs549095193
Varsome	rs549095193
LitVar	rs549095193
Map	rs549095193
PheGenI	rs549095193
Biobank	rs549095193
1000 genomes	rs549095193
hgdp	rs549095193
ensembl	rs549095193
geneview	rs549095193
scholar	rs549095193
google	rs549095193
pharmgkb	rs549095193
gwascentral	rs549095193
openSNP	rs549095193
23andMe	rs549095193
SNPshot	rs549095193
SNPdbe	rs549095193
MSV3d	rs549095193
GWAS Ctlg	rs549095193

Max Magnitude

0

ClinVar
Risk	rs549095193(A;A) rs549095193(T;T)
Alt	rs549095193(A;A) rs549095193(T;T)
Reference	Rs549095193(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TRIOBP
CLNDBN	Deafness, autosomal recessive 28
Reversed	0
HGVS	NC_000022.10:g.38121618G>A
CLNSRC
CLNACC	RCV000454135.1,