rs121909595

Orientation

minus

Stabilized

minus

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

Make rs121909595(C;T)

Make rs121909595(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

208124321

Gene	CRYGD, LOC100507443

is a	snp
is	mentioned by
dbSNP	rs121909595
dbSNP (classic)	rs121909595
ClinGen	rs121909595
ebi	rs121909595
HLI	rs121909595
Exac	rs121909595
Gnomad	rs121909595
Varsome	rs121909595
LitVar	rs121909595
Map	rs121909595
PheGenI	rs121909595
Biobank	rs121909595
1000 genomes	rs121909595
hgdp	rs121909595
ensembl	rs121909595
geneview	rs121909595
scholar	rs121909595
google	rs121909595
pharmgkb	rs121909595
gwascentral	rs121909595
openSNP	rs121909595
23andMe	rs121909595
SNPshot	rs121909595
SNPdbe	rs121909595
MSV3d	rs121909595
GWAS Ctlg	rs121909595

Max Magnitude

0

OMIM	123690
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909595(T;T)
Alt	rs121909595(T;T)
Reference	Rs121909595(C;C)
Significance	Pathogenic
Disease	Cataract 4
Variation	info
Gene	CRYGD LOC100507443
CLNDBN	Cataract 4
Reversed	1
HGVS	NC_000002.11:g.208989045G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018445.30,