rs137853199

Orientation

minus

Stabilized

minus

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

Make rs137853199(G;T)

Make rs137853199(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

16125304

Gene

EPHA2

is a	snp
is	mentioned by
dbSNP	rs137853199
dbSNP (classic)	rs137853199
ClinGen	rs137853199
ebi	rs137853199
HLI	rs137853199
Exac	rs137853199
Gnomad	rs137853199
Varsome	rs137853199
LitVar	rs137853199
Map	rs137853199
PheGenI	rs137853199
Biobank	rs137853199
1000 genomes	rs137853199
hgdp	rs137853199
ensembl	rs137853199
geneview	rs137853199
scholar	rs137853199
google	rs137853199
pharmgkb	rs137853199
gwascentral	rs137853199
openSNP	rs137853199
23andMe	rs137853199
SNPshot	rs137853199
SNPdbe	rs137853199
MSV3d	rs137853199
GWAS Ctlg	rs137853199

Max Magnitude

0

OMIM	176946
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137853199(T;T)
Alt	rs137853199(T;T)
Reference	Rs137853199(G;G)
Significance	Pathogenic
Disease	Cataract 6
Variation	info
Gene	EPHA2
CLNDBN	Cataract 6, multiple types
Reversed	1
HGVS	NC_000001.10:g.16451799C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014168.24,