rs267607153

Orientation

minus

Stabilized

minus

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

Make rs267607153(A;A)

Make rs267607153(A;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

120810512

Gene

TSPAN12

is a	snp
is	mentioned by
dbSNP	rs267607153
dbSNP (classic)	rs267607153
ClinGen	rs267607153
ebi	rs267607153
HLI	rs267607153
Exac	rs267607153
Gnomad	rs267607153
Varsome	rs267607153
LitVar	rs267607153
Map	rs267607153
PheGenI	rs267607153
Biobank	rs267607153
1000 genomes	rs267607153
hgdp	rs267607153
ensembl	rs267607153
geneview	rs267607153
scholar	rs267607153
google	rs267607153
pharmgkb	rs267607153
gwascentral	rs267607153
openSNP	rs267607153
23andMe	rs267607153
SNPshot	rs267607153
SNPdbe	rs267607153
MSV3d	rs267607153
GWAS Ctlg	rs267607153

Max Magnitude

0

ClinVar
Risk	rs267607153(A;A)
Alt	rs267607153(A;A)
Reference	Rs267607153(T;T)
Significance	Pathogenic
Disease	Exudative vitreoretinopathy 5
Variation	info
Gene	TSPAN12
CLNDBN	Exudative vitreoretinopathy 5
Reversed	1
HGVS	NC_000007.13:g.120450566A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000350.5,