rs766589610

Orientation

plus

Stabilized

plus

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

Make rs766589610(C;T)

Make rs766589610(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

68357846

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs766589610
dbSNP (classic)	rs766589610
ClinGen	rs766589610
ebi	rs766589610
HLI	rs766589610
Exac	rs766589610
Gnomad	rs766589610
Varsome	rs766589610
LitVar	rs766589610
Map	rs766589610
PheGenI	rs766589610
Biobank	rs766589610
1000 genomes	rs766589610
hgdp	rs766589610
ensembl	rs766589610
geneview	rs766589610
scholar	rs766589610
google	rs766589610
pharmgkb	rs766589610
gwascentral	rs766589610
openSNP	rs766589610
23andMe	rs766589610
SNPshot	rs766589610
SNPdbe	rs766589610
MSV3d	rs766589610
GWAS Ctlg	rs766589610

Max Magnitude

0

ClinVar
Risk	rs766589610(T;T)
Alt	rs766589610(T;T)
Reference	Rs766589610(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LRP5
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.68125314C>T
CLNSRC
CLNACC	RCV000171198.1,