rs794726661

Orientation

minus

Stabilized

minus

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

Make rs794726661(A;G)

Make rs794726661(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

31790862

Gene

PAX6

is a	snp
is	mentioned by
dbSNP	rs794726661
dbSNP (classic)	rs794726661
ClinGen	rs794726661
ebi	rs794726661
HLI	rs794726661
Exac	rs794726661
Gnomad	rs794726661
Varsome	rs794726661
LitVar	rs794726661
Map	rs794726661
PheGenI	rs794726661
Biobank	rs794726661
1000 genomes	rs794726661
hgdp	rs794726661
ensembl	rs794726661
geneview	rs794726661
scholar	rs794726661
google	rs794726661
pharmgkb	rs794726661
gwascentral	rs794726661
openSNP	rs794726661
23andMe	rs794726661
SNPshot	rs794726661
SNPdbe	rs794726661
MSV3d	rs794726661
GWAS Ctlg	rs794726661

Max Magnitude

0

ClinVar
Risk	rs794726661(G;G)
Alt	rs794726661(G;G)
Reference	Rs794726661(A;A)
Significance	Pathogenic
Disease	Aniridia 1 not provided
Variation	info
Gene	PAX6
CLNDBN	Aniridia 1 not provided
Reversed	1
HGVS	NC_000011.9:g.31812410T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003633.4, RCV000414592.1,