rs387906966

Orientation

minus

Stabilized

minus

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

Make rs387906966(C;T)

Make rs387906966(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

45967788

Gene

FYCO1

is a	snp
is	mentioned by
dbSNP	rs387906966
dbSNP (classic)	rs387906966
ClinGen	rs387906966
ebi	rs387906966
HLI	rs387906966
Exac	rs387906966
Gnomad	rs387906966
Varsome	rs387906966
LitVar	rs387906966
Map	rs387906966
PheGenI	rs387906966
Biobank	rs387906966
1000 genomes	rs387906966
hgdp	rs387906966
ensembl	rs387906966
geneview	rs387906966
scholar	rs387906966
google	rs387906966
pharmgkb	rs387906966
gwascentral	rs387906966
openSNP	rs387906966
23andMe	rs387906966
SNPshot	rs387906966
SNPdbe	rs387906966
MSV3d	rs387906966
GWAS Ctlg	rs387906966

Max Magnitude

0

ClinVar
Risk	rs387906966(T;T)
Alt	rs387906966(T;T)
Reference	Rs387906966(C;C)
Significance	Pathogenic
Disease	Cataract
Variation	info
Gene	FYCO1
CLNDBN	Cataract, autosomal recessive congenital 2
Reversed	1
HGVS	NC_000003.11:g.46009280G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023625.3,