rs104893618

Orientation

minus

Stabilized

minus

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

Make rs104893618(A;C)

Make rs104893618(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

208129680

Gene	CRYGC, LOC100507443

is a	snp
is	mentioned by
dbSNP	rs104893618
dbSNP (classic)	rs104893618
ClinGen	rs104893618
ebi	rs104893618
HLI	rs104893618
Exac	rs104893618
Gnomad	rs104893618
Varsome	rs104893618
LitVar	rs104893618
Map	rs104893618
PheGenI	rs104893618
Biobank	rs104893618
1000 genomes	rs104893618
hgdp	rs104893618
ensembl	rs104893618
geneview	rs104893618
scholar	rs104893618
google	rs104893618
pharmgkb	rs104893618
gwascentral	rs104893618
openSNP	rs104893618
23andMe	rs104893618
SNPshot	rs104893618
SNPdbe	rs104893618
MSV3d	rs104893618
GWAS Ctlg	rs104893618

Max Magnitude

0

OMIM	123680
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893618(C;C)
Alt	rs104893618(C;C)
Reference	Rs104893618(A;A)
Significance	Pathogenic
Disease	Cataract 2
Variation	info
Gene	CRYGC LOC100507443
CLNDBN	Cataract 2, Coppock-like
Reversed	1
HGVS	NC_000002.11:g.208994404T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018452.28,