rs527236079

Orientation

plus

Stabilized

plus

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

Make rs527236079(C;T)

Make rs527236079(T;T)

Reference

GRCh38 38.1/142

Chromosome

4

Position

154744489

Gene

LRAT

is a	snp
is	mentioned by
dbSNP	rs527236079
dbSNP (classic)	rs527236079
ClinGen	rs527236079
ebi	rs527236079
HLI	rs527236079
Exac	rs527236079
Gnomad	rs527236079
Varsome	rs527236079
LitVar	rs527236079
Map	rs527236079
PheGenI	rs527236079
Biobank	rs527236079
1000 genomes	rs527236079
hgdp	rs527236079
ensembl	rs527236079
geneview	rs527236079
scholar	rs527236079
google	rs527236079
pharmgkb	rs527236079
gwascentral	rs527236079
openSNP	rs527236079
23andMe	rs527236079
SNPshot	rs527236079
SNPdbe	rs527236079
MSV3d	rs527236079
GWAS Ctlg	rs527236079

Max Magnitude

0

ClinVar
Risk	rs527236079(T;T)
Alt	rs527236079(T;T)
Reference	Rs527236079(C;C)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa
Variation	info
Gene	LRAT
CLNDBN	Retinitis pigmentosa
Reversed	0
HGVS	NC_000004.11:g.155665641C>T
CLNSRC	ClinVar
CLNACC	RCV000132653.1,