rs267607033

Orientation

plus

Stabilized

plus

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

Make rs267607033(C;C)

Make rs267607033(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156162993

Gene

SEMA4A

is a	snp
is	mentioned by
dbSNP	rs267607033
dbSNP (classic)	rs267607033
ClinGen	rs267607033
ebi	rs267607033
HLI	rs267607033
Exac	rs267607033
Gnomad	rs267607033
Varsome	rs267607033
LitVar	rs267607033
Map	rs267607033
PheGenI	rs267607033
Biobank	rs267607033
1000 genomes	rs267607033
hgdp	rs267607033
ensembl	rs267607033
geneview	rs267607033
scholar	rs267607033
google	rs267607033
pharmgkb	rs267607033
gwascentral	rs267607033
openSNP	rs267607033
23andMe	rs267607033
SNPshot	rs267607033
SNPdbe	rs267607033
MSV3d	rs267607033
GWAS Ctlg	rs267607033

Max Magnitude

0

ClinVar
Risk	rs267607033(C;C)
Alt	rs267607033(C;C)
Reference	Rs267607033(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 35 Cone-rod dystrophy 10
Variation	info
Gene	SEMA4A
CLNDBN	Retinitis pigmentosa 35 Cone-rod dystrophy 10
Reversed	0
HGVS	NC_000001.10:g.156132784G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003524.3, RCV000003525.3,