rs786205534

Orientation

plus

Stabilized

plus

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

Make rs786205534(G;G)

Make rs786205534(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

111997478

Gene

MERTK

is a	snp
is	mentioned by
dbSNP	rs786205534
dbSNP (classic)	rs786205534
ClinGen	rs786205534
ebi	rs786205534
HLI	rs786205534
Exac	rs786205534
Gnomad	rs786205534
Varsome	rs786205534
LitVar	rs786205534
Map	rs786205534
PheGenI	rs786205534
Biobank	rs786205534
1000 genomes	rs786205534
hgdp	rs786205534
ensembl	rs786205534
geneview	rs786205534
scholar	rs786205534
google	rs786205534
pharmgkb	rs786205534
gwascentral	rs786205534
openSNP	rs786205534
23andMe	rs786205534
SNPshot	rs786205534
SNPdbe	rs786205534
MSV3d	rs786205534
GWAS Ctlg	rs786205534

Max Magnitude

0

aka c.1604+2T>G

ClinVar
Risk	rs786205534(G;G)
Alt	rs786205534(G;G)
Reference	Rs786205534(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MERTK
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.112755055T>G
CLNSRC
CLNACC	RCV000171304.1,