rs797045107

Orientation

minus

Stabilized

minus

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

Make rs797045107(C;C)

Make rs797045107(C;GCTTCGCCA)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

3234173

Gene

SLC4A11

is a	snp
is	mentioned by
dbSNP	rs797045107
dbSNP (classic)	rs797045107
ClinGen	rs797045107
ebi	rs797045107
HLI	rs797045107
Exac	rs797045107
Gnomad	rs797045107
Varsome	rs797045107
LitVar	rs797045107
Map	rs797045107
PheGenI	rs797045107
Biobank	rs797045107
1000 genomes	rs797045107
hgdp	rs797045107
ensembl	rs797045107
geneview	rs797045107
scholar	rs797045107
google	rs797045107
pharmgkb	rs797045107
gwascentral	rs797045107
openSNP	rs797045107
23andMe	rs797045107
SNPshot	rs797045107
SNPdbe	rs797045107
MSV3d	rs797045107
GWAS Ctlg	rs797045107

Max Magnitude

0

ClinVar
Risk	rs797045107(C;C)
Alt	rs797045107(C;C)
Reference	Rs797045107(GCTTCGCCA;GCTTCGCCA)
Significance	Pathogenic
Disease	Corneal endothelial dystrophy type 2
Variation	info
Gene	SLC4A11
CLNDBN	Corneal endothelial dystrophy type 2
Reversed	1
HGVS	NC_000020.10:g.3214819_3214827delinsG
CLNSRC
CLNACC	RCV000190625.1,