rs121909396

Orientation

minus

Stabilized

minus

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

Make rs121909396(A;G)

Make rs121909396(G;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3228299

Gene

SLC4A11

is a	snp
is	mentioned by
dbSNP	rs121909396
dbSNP (classic)	rs121909396
ClinGen	rs121909396
ebi	rs121909396
HLI	rs121909396
Exac	rs121909396
Gnomad	rs121909396
Varsome	rs121909396
LitVar	rs121909396
Map	rs121909396
PheGenI	rs121909396
Biobank	rs121909396
1000 genomes	rs121909396
hgdp	rs121909396
ensembl	rs121909396
geneview	rs121909396
scholar	rs121909396
google	rs121909396
pharmgkb	rs121909396
gwascentral	rs121909396
openSNP	rs121909396
23andMe	rs121909396
SNPshot	rs121909396
SNPdbe	rs121909396
MSV3d	rs121909396
GWAS Ctlg	rs121909396

Max Magnitude

0

OMIM	610206
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121909396(G;G)
Alt	rs121909396(G;G)
Reference	Rs121909396(A;A)
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.3208945T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001378.3,