rs864309701

Orientation

minus

Stabilized

minus

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

Make rs864309701(-;G)

Make rs864309701(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

208121749

Gene	CRYGD, LOC100507443

is a	snp
is	mentioned by
dbSNP	rs864309701
dbSNP (classic)	rs864309701
ClinGen	rs864309701
ebi	rs864309701
HLI	rs864309701
Exac	rs864309701
Gnomad	rs864309701
Varsome	rs864309701
LitVar	rs864309701
Map	rs864309701
PheGenI	rs864309701
Biobank	rs864309701
1000 genomes	rs864309701
hgdp	rs864309701
ensembl	rs864309701
geneview	rs864309701
scholar	rs864309701
google	rs864309701
pharmgkb	rs864309701
gwascentral	rs864309701
openSNP	rs864309701
23andMe	rs864309701
SNPshot	rs864309701
SNPdbe	rs864309701
MSV3d	rs864309701
GWAS Ctlg	rs864309701

Max Magnitude

0

ClinVar
Risk	rs864309701(G;G)
Alt	rs864309701(G;G)
Reference	Rs864309701(-;-)
Significance	Pathogenic
Disease	Congenital cataract
Variation	info
Gene	CRYGD LOC100507443
CLNDBN	Congenital cataract
Reversed	1
HGVS	NC_000002.11:g.208986474dupC
CLNSRC
CLNACC	RCV000203375.1,