rs118204026

Orientation

plus

Stabilized

plus

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

Make rs118204026(C;T)

Make rs118204026(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

37723595

Gene

TRIOBP

is a	snp
is	mentioned by
dbSNP	rs118204026
dbSNP (classic)	rs118204026
ClinGen	rs118204026
ebi	rs118204026
HLI	rs118204026
Exac	rs118204026
Gnomad	rs118204026
Varsome	rs118204026
LitVar	rs118204026
Map	rs118204026
PheGenI	rs118204026
Biobank	rs118204026
1000 genomes	rs118204026
hgdp	rs118204026
ensembl	rs118204026
geneview	rs118204026
scholar	rs118204026
google	rs118204026
pharmgkb	rs118204026
gwascentral	rs118204026
openSNP	rs118204026
23andMe	rs118204026
SNPshot	rs118204026
SNPdbe	rs118204026
MSV3d	rs118204026
GWAS Ctlg	rs118204026

Max Magnitude

0

OMIM	609761
Desc
Variant	0001
Related	also

ClinVar
Risk	rs118204026(G;G) rs118204026(T;T)
Alt	rs118204026(G;G) rs118204026(T;T)
Reference	Rs118204026(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TRIOBP
CLNDBN	Deafness, autosomal recessive 28
Reversed	0
HGVS	NC_000022.10:g.38119602C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001555.4,