rs1060499809

Orientation

plus

Stabilized

plus

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

Make rs1060499809(C;T)

Make rs1060499809(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

37724003

Gene

TRIOBP

is a	snp
is	mentioned by
dbSNP	rs1060499809
dbSNP (classic)	rs1060499809
ClinGen	rs1060499809
ebi	rs1060499809
HLI	rs1060499809
Exac	rs1060499809
Gnomad	rs1060499809
Varsome	rs1060499809
LitVar	rs1060499809
Map	rs1060499809
PheGenI	rs1060499809
Biobank	rs1060499809
1000 genomes	rs1060499809
hgdp	rs1060499809
ensembl	rs1060499809
geneview	rs1060499809
scholar	rs1060499809
google	rs1060499809
pharmgkb	rs1060499809
gwascentral	rs1060499809
openSNP	rs1060499809
23andMe	rs1060499809
SNPshot	rs1060499809
SNPdbe	rs1060499809
MSV3d	rs1060499809
GWAS Ctlg	rs1060499809

Max Magnitude

0

ClinVar
Risk	rs1060499809(T;T)
Alt	rs1060499809(T;T)
Reference	Rs1060499809(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TRIOBP
CLNDBN	Deafness, autosomal recessive 28
Reversed	0
HGVS	NC_000022.10:g.38120010C>T
CLNSRC
CLNACC	RCV000454233.1,