rs74315508

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs74315508(C;T)

Make rs74315508(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

20242778

Gene

RTN4R

is a	snp
is	mentioned by
dbSNP	rs74315508
dbSNP (classic)	rs74315508
ClinGen	rs74315508
ebi	rs74315508
HLI	rs74315508
Exac	rs74315508
Gnomad	rs74315508
Varsome	rs74315508
LitVar	rs74315508
Map	rs74315508
PheGenI	rs74315508
Biobank	rs74315508
1000 genomes	rs74315508
hgdp	rs74315508
ensembl	rs74315508
geneview	rs74315508
scholar	rs74315508
google	rs74315508
pharmgkb	rs74315508
gwascentral	rs74315508
openSNP	rs74315508
23andMe	rs74315508
SNPshot	rs74315508
SNPdbe	rs74315508
MSV3d	rs74315508
GWAS Ctlg	rs74315508

GMAF

0.003214

Max Magnitude

0

OMIM	605566
Desc
Variant	0001
Related	also

ClinVar
Risk	rs74315508(G;G) rs74315508(T;T)
Alt	rs74315508(G;G) rs74315508(T;T)
Reference	Rs74315508(C;C)
Significance	Other
Disease	Schizophrenia
Variation	info
Gene	RTN4R
CLNDBN	Schizophrenia, susceptibility to
Reversed	1
HGVS	NC_000022.10:g.20230301G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005158.3,