rs527236134

Orientation

plus

Stabilized

plus

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

Make rs527236134(C;T)

Make rs527236134(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

111929428

Gene

MERTK

is a	snp
is	mentioned by
dbSNP	rs527236134
dbSNP (classic)	rs527236134
ClinGen	rs527236134
ebi	rs527236134
HLI	rs527236134
Exac	rs527236134
Gnomad	rs527236134
Varsome	rs527236134
LitVar	rs527236134
Map	rs527236134
PheGenI	rs527236134
Biobank	rs527236134
1000 genomes	rs527236134
hgdp	rs527236134
ensembl	rs527236134
geneview	rs527236134
scholar	rs527236134
google	rs527236134
pharmgkb	rs527236134
gwascentral	rs527236134
openSNP	rs527236134
23andMe	rs527236134
SNPshot	rs527236134
SNPdbe	rs527236134
MSV3d	rs527236134
GWAS Ctlg	rs527236134

Max Magnitude

0

ClinVar
Risk	rs527236134(T;T)
Alt	rs527236134(T;T)
Reference	Rs527236134(C;C)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa 38
Variation	info
Gene	MERTK
CLNDBN	Retinitis pigmentosa 38
Reversed	0
HGVS	NC_000002.11:g.112687005C>T
CLNSRC	ClinVar
CLNACC	RCV000132665.1,