rs540911439

Orientation

plus

Stabilized

plus

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

Make rs540911439(C;T)

Make rs540911439(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

89191358

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs540911439
dbSNP (classic)	rs540911439
ClinGen	rs540911439
ebi	rs540911439
HLI	rs540911439
Exac	rs540911439
Gnomad	rs540911439
Varsome	rs540911439
LitVar	rs540911439
Map	rs540911439
PheGenI	rs540911439
Biobank	rs540911439
1000 genomes	rs540911439
hgdp	rs540911439
ensembl	rs540911439
geneview	rs540911439
scholar	rs540911439
google	rs540911439
pharmgkb	rs540911439
gwascentral	rs540911439
openSNP	rs540911439
23andMe	rs540911439
SNPshot	rs540911439
SNPdbe	rs540911439
MSV3d	rs540911439
GWAS Ctlg	rs540911439

Max Magnitude

0

ClinVar
Risk	rs540911439(T;T)
Alt	rs540911439(T;T)
Reference	Rs540911439(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TYR
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.88924526C>T
CLNSRC
CLNACC	RCV000429411.1,