rs886043389

Orientation

plus

Stabilized

plus

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

Chromosome

22

Position

37726410

Gene

TRIOBP

is a	snp
is	mentioned by
dbSNP	rs886043389
dbSNP (classic)	rs886043389
ClinGen	rs886043389
ebi	rs886043389
HLI	rs886043389
Exac	rs886043389
Gnomad	rs886043389
Varsome	rs886043389
LitVar	rs886043389
Map	rs886043389
PheGenI	rs886043389
Biobank	rs886043389
1000 genomes	rs886043389
hgdp	rs886043389
ensembl	rs886043389
geneview	rs886043389
scholar	rs886043389
google	rs886043389
pharmgkb	rs886043389
gwascentral	rs886043389
openSNP	rs886043389
23andMe	rs886043389
SNPshot	rs886043389
SNPdbe	rs886043389
MSV3d	rs886043389
GWAS Ctlg	rs886043389

Max Magnitude

0

ClinVar
Risk	rs886043389(-;-)
Alt	rs886043389(-;-)
Reference	Rs886043389(AG;AG)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	TRIOBP
CLNDBN	Deafness, autosomal recessive 28
Reversed	0
HGVS	NC_000022.10:g.38122417_38122418delGA
CLNSRC
CLNACC	RCV000267345.1,