rs267607110

Orientation

plus

Stabilized

plus

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

Make rs267607110(A;A)

Make rs267607110(A;C)

Reference

GRCh38 38.1/141

Chromosome

5

Position

136056769

Gene

TGFBI

is a	snp
is	mentioned by
dbSNP	rs267607110
dbSNP (classic)	rs267607110
ClinGen	rs267607110
ebi	rs267607110
HLI	rs267607110
Exac	rs267607110
Gnomad	rs267607110
Varsome	rs267607110
LitVar	rs267607110
Map	rs267607110
PheGenI	rs267607110
Biobank	rs267607110
1000 genomes	rs267607110
hgdp	rs267607110
ensembl	rs267607110
geneview	rs267607110
scholar	rs267607110
google	rs267607110
pharmgkb	rs267607110
gwascentral	rs267607110
openSNP	rs267607110
23andMe	rs267607110
SNPshot	rs267607110
SNPdbe	rs267607110
MSV3d	rs267607110
GWAS Ctlg	rs267607110

Max Magnitude

0

ClinVar
Risk	rs267607110(A;A)
Alt	rs267607110(A;A)
Reference	Rs267607110(C;C)
Significance	Pathogenic
Disease	Lattice corneal dystrophy Type I
Variation	info
Gene	TGFBI
CLNDBN	Lattice corneal dystrophy Type I
Reversed	0
HGVS	NC_000005.9:g.135392458C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008323.3,