rs1057518737

Orientation

plus

Stabilized

plus

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

Make rs1057518737(C;G)

Make rs1057518737(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

47416666

Gene	FOXE3, LINC01389

is a	snp
is	mentioned by
dbSNP	rs1057518737
dbSNP (classic)	rs1057518737
ClinGen	rs1057518737
ebi	rs1057518737
HLI	rs1057518737
Exac	rs1057518737
Gnomad	rs1057518737
Varsome	rs1057518737
LitVar	rs1057518737
Map	rs1057518737
PheGenI	rs1057518737
Biobank	rs1057518737
1000 genomes	rs1057518737
hgdp	rs1057518737
ensembl	rs1057518737
geneview	rs1057518737
scholar	rs1057518737
google	rs1057518737
pharmgkb	rs1057518737
gwascentral	rs1057518737
openSNP	rs1057518737
23andMe	rs1057518737
SNPshot	rs1057518737
SNPdbe	rs1057518737
MSV3d	rs1057518737
GWAS Ctlg	rs1057518737

Max Magnitude

0

ClinVar
Risk	rs1057518737(G;G)
Alt	rs1057518737(G;G)
Reference	Rs1057518737(C;C)
Significance	Pathogenic
Disease	Cataract 34
Variation	info
Gene	FOXE3
CLNDBN	Cataract 34, multiple types
Reversed	0
HGVS	NC_000001.10:g.47882338C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000412651.1,