rs121909395

Orientation

minus

Stabilized

minus

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

Make rs121909395(C;C)

Make rs121909395(C;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3233937

Gene

SLC4A11

is a	snp
is	mentioned by
dbSNP	rs121909395
dbSNP (classic)	rs121909395
ClinGen	rs121909395
ebi	rs121909395
HLI	rs121909395
Exac	rs121909395
Gnomad	rs121909395
Varsome	rs121909395
LitVar	rs121909395
Map	rs121909395
PheGenI	rs121909395
Biobank	rs121909395
1000 genomes	rs121909395
hgdp	rs121909395
ensembl	rs121909395
geneview	rs121909395
scholar	rs121909395
google	rs121909395
pharmgkb	rs121909395
gwascentral	rs121909395
openSNP	rs121909395
23andMe	rs121909395
SNPshot	rs121909395
SNPdbe	rs121909395
MSV3d	rs121909395
GWAS Ctlg	rs121909395

Max Magnitude

0

OMIM	610206
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121909395(C;C)
Alt	rs121909395(C;C)
Reference	Rs121909395(T;T)
Significance	Pathogenic
Disease	Corneal dystrophy and perceptive deafness
Variation	info
Gene	SLC4A11
CLNDBN	Corneal dystrophy and perceptive deafness
Reversed	1
HGVS	NC_000020.10:g.3214583A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001382.4,