rs1057517782

Orientation

minus

Stabilized

minus

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

Make rs1057517782(G;G)

Make rs1057517782(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

31802702

Gene

PAX6

is a	snp
is	mentioned by
dbSNP	rs1057517782
dbSNP (classic)	rs1057517782
ClinGen	rs1057517782
ebi	rs1057517782
HLI	rs1057517782
Exac	rs1057517782
Gnomad	rs1057517782
Varsome	rs1057517782
LitVar	rs1057517782
Map	rs1057517782
PheGenI	rs1057517782
Biobank	rs1057517782
1000 genomes	rs1057517782
hgdp	rs1057517782
ensembl	rs1057517782
geneview	rs1057517782
scholar	rs1057517782
google	rs1057517782
pharmgkb	rs1057517782
gwascentral	rs1057517782
openSNP	rs1057517782
23andMe	rs1057517782
SNPshot	rs1057517782
SNPdbe	rs1057517782
MSV3d	rs1057517782
GWAS Ctlg	rs1057517782

Max Magnitude

0

ClinVar
Risk	rs1057517782(G;G)
Alt	rs1057517782(G;G)
Reference	Rs1057517782(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAX6
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.31824250A>C
CLNSRC
CLNACC	RCV000413692.1,