rs118204027

Orientation

plus

Stabilized

plus

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

Make rs118204027(C;T)

Make rs118204027(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

37724297

Gene

TRIOBP

is a	snp
is	mentioned by
dbSNP	rs118204027
dbSNP (classic)	rs118204027
ClinGen	rs118204027
ebi	rs118204027
HLI	rs118204027
Exac	rs118204027
Gnomad	rs118204027
Varsome	rs118204027
LitVar	rs118204027
Map	rs118204027
PheGenI	rs118204027
Biobank	rs118204027
1000 genomes	rs118204027
hgdp	rs118204027
ensembl	rs118204027
geneview	rs118204027
scholar	rs118204027
google	rs118204027
pharmgkb	rs118204027
gwascentral	rs118204027
openSNP	rs118204027
23andMe	rs118204027
SNPshot	rs118204027
SNPdbe	rs118204027
MSV3d	rs118204027
GWAS Ctlg	rs118204027

Max Magnitude

0

OMIM	609761
Desc
Variant	0002
Related	also

ClinVar
Risk	rs118204027(T;T)
Alt	rs118204027(T;T)
Reference	Rs118204027(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TRIOBP
CLNDBN	Deafness, autosomal recessive 28
Reversed	0
HGVS	NC_000022.10:g.38120304C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001556.3,