rs267607034

Orientation

plus

Stabilized

plus

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

Make rs267607034(G;G)

Make rs267607034(G;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156163009

Gene

SEMA4A

is a	snp
is	mentioned by
dbSNP	rs267607034
dbSNP (classic)	rs267607034
ClinGen	rs267607034
ebi	rs267607034
HLI	rs267607034
Exac	rs267607034
Gnomad	rs267607034
Varsome	rs267607034
LitVar	rs267607034
Map	rs267607034
PheGenI	rs267607034
Biobank	rs267607034
1000 genomes	rs267607034
hgdp	rs267607034
ensembl	rs267607034
geneview	rs267607034
scholar	rs267607034
google	rs267607034
pharmgkb	rs267607034
gwascentral	rs267607034
openSNP	rs267607034
23andMe	rs267607034
SNPshot	rs267607034
SNPdbe	rs267607034
MSV3d	rs267607034
GWAS Ctlg	rs267607034

Max Magnitude

0

ClinVar
Risk	rs267607034(G;G)
Alt	rs267607034(G;G)
Reference	Rs267607034(T;T)
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.156132800T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003526.3, RCV000003527.3,