rs118204030

Orientation

plus

Stabilized

plus

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

Make rs118204030(C;T)

Make rs118204030(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

37725758

Gene

TRIOBP

is a	snp
is	mentioned by
dbSNP	rs118204030
dbSNP (classic)	rs118204030
ClinGen	rs118204030
ebi	rs118204030
HLI	rs118204030
Exac	rs118204030
Gnomad	rs118204030
Varsome	rs118204030
LitVar	rs118204030
Map	rs118204030
PheGenI	rs118204030
Biobank	rs118204030
1000 genomes	rs118204030
hgdp	rs118204030
ensembl	rs118204030
geneview	rs118204030
scholar	rs118204030
google	rs118204030
pharmgkb	rs118204030
gwascentral	rs118204030
openSNP	rs118204030
23andMe	rs118204030
SNPshot	rs118204030
SNPdbe	rs118204030
MSV3d	rs118204030
GWAS Ctlg	rs118204030

Max Magnitude

0

OMIM	609761
Desc
Variant	0005
Related	also

ClinVar
Risk	rs118204030(T;T)
Alt	rs118204030(T;T)
Reference	Rs118204030(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TRIOBP
CLNDBN	Deafness, autosomal recessive 28
Reversed	0
HGVS	NC_000022.10:g.38121765C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001559.3,