rs121909388

Orientation

minus

Stabilized

minus

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

Make rs121909388(C;T)

Make rs121909388(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3230258

Gene

SLC4A11

is a	snp
is	mentioned by
dbSNP	rs121909388
dbSNP (classic)	rs121909388
ClinGen	rs121909388
ebi	rs121909388
HLI	rs121909388
Exac	rs121909388
Gnomad	rs121909388
Varsome	rs121909388
LitVar	rs121909388
Map	rs121909388
PheGenI	rs121909388
Biobank	rs121909388
1000 genomes	rs121909388
hgdp	rs121909388
ensembl	rs121909388
geneview	rs121909388
scholar	rs121909388
google	rs121909388
pharmgkb	rs121909388
gwascentral	rs121909388
openSNP	rs121909388
23andMe	rs121909388
SNPshot	rs121909388
SNPdbe	rs121909388
MSV3d	rs121909388
GWAS Ctlg	rs121909388

Max Magnitude

0

OMIM	610206
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909388(T;T)
Alt	rs121909388(T;T)
Reference	Rs121909388(C;C)
Significance	Pathogenic
Disease	Corneal endothelial dystrophy
Variation	info
Gene	SLC4A11
CLNDBN	Corneal endothelial dystrophy
Reversed	1
HGVS	NC_000020.10:g.3210904G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001368.3,