rs770383372

Orientation

plus

Stabilized

plus

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

Make rs770383372(G;T)

Make rs770383372(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

68357661

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs770383372
dbSNP (classic)	rs770383372
ClinGen	rs770383372
ebi	rs770383372
HLI	rs770383372
Exac	rs770383372
Gnomad	rs770383372
Varsome	rs770383372
LitVar	rs770383372
Map	rs770383372
PheGenI	rs770383372
Biobank	rs770383372
1000 genomes	rs770383372
hgdp	rs770383372
ensembl	rs770383372
geneview	rs770383372
scholar	rs770383372
google	rs770383372
pharmgkb	rs770383372
gwascentral	rs770383372
openSNP	rs770383372
23andMe	rs770383372
SNPshot	rs770383372
SNPdbe	rs770383372
MSV3d	rs770383372
GWAS Ctlg	rs770383372

Max Magnitude

0

ClinVar
Risk	rs770383372(C;C) rs770383372(T;T)
Alt	rs770383372(C;C) rs770383372(T;T)
Reference	Rs770383372(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	LRP5
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000011.9:g.68125129G>C
CLNSRC
CLNACC	RCV000190810.1,