rs121913555

Orientation

minus

Stabilized

minus

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

Make rs121913555(G;G)

Make rs121913555(G;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

51382430

Gene

LIM2

is a	snp
is	mentioned by
dbSNP	rs121913555
dbSNP (classic)	rs121913555
ClinGen	rs121913555
ebi	rs121913555
HLI	rs121913555
Exac	rs121913555
Gnomad	rs121913555
Varsome	rs121913555
LitVar	rs121913555
Map	rs121913555
PheGenI	rs121913555
Biobank	rs121913555
1000 genomes	rs121913555
hgdp	rs121913555
ensembl	rs121913555
geneview	rs121913555
scholar	rs121913555
google	rs121913555
pharmgkb	rs121913555
gwascentral	rs121913555
openSNP	rs121913555
23andMe	rs121913555
SNPshot	rs121913555
SNPdbe	rs121913555
MSV3d	rs121913555
GWAS Ctlg	rs121913555

Max Magnitude

0

OMIM	154045
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121913555(G;G)
Alt	rs121913555(G;G)
Reference	Rs121913555(T;T)
Significance	Pathogenic
Disease	Cataract 19
Variation	info
Gene	LIM2
CLNDBN	Cataract 19, multiple types
Reversed	1
HGVS	NC_000019.9:g.51885684A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015430.23,