rs121909389

Orientation

minus

Stabilized

minus

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

Make rs121909389(A;A)

Make rs121909389(A;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3230587

Gene

SLC4A11

is a	snp
is	mentioned by
dbSNP	rs121909389
dbSNP (classic)	rs121909389
ClinGen	rs121909389
ebi	rs121909389
HLI	rs121909389
Exac	rs121909389
Gnomad	rs121909389
Varsome	rs121909389
LitVar	rs121909389
Map	rs121909389
PheGenI	rs121909389
Biobank	rs121909389
1000 genomes	rs121909389
hgdp	rs121909389
ensembl	rs121909389
geneview	rs121909389
scholar	rs121909389
google	rs121909389
pharmgkb	rs121909389
gwascentral	rs121909389
openSNP	rs121909389
23andMe	rs121909389
SNPshot	rs121909389
SNPdbe	rs121909389
MSV3d	rs121909389
GWAS Ctlg	rs121909389

Max Magnitude

0

OMIM	610206
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909389(A;A)
Alt	rs121909389(A;A)
Reference	Rs121909389(G;G)
Significance	Pathogenic
Disease	Corneal endothelial dystrophy
Variation	info
Gene	SLC4A11
CLNDBN	Corneal endothelial dystrophy
Reversed	1
HGVS	NC_000020.10:g.3211233C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001369.3,