rs80338852

Orientation

plus

Stabilized

plus

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

Make rs80338852(A;A)

Make rs80338852(A;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

31317599

Gene

B3GLCT

is a	snp
is	mentioned by
dbSNP	rs80338852
dbSNP (classic)	rs80338852
ClinGen	rs80338852
ebi	rs80338852
HLI	rs80338852
Exac	rs80338852
Gnomad	rs80338852
Varsome	rs80338852
LitVar	rs80338852
Map	rs80338852
PheGenI	rs80338852
Biobank	rs80338852
1000 genomes	rs80338852
hgdp	rs80338852
ensembl	rs80338852
geneview	rs80338852
scholar	rs80338852
google	rs80338852
pharmgkb	rs80338852
gwascentral	rs80338852
openSNP	rs80338852
23andMe	rs80338852
SNPshot	rs80338852
SNPdbe	rs80338852
MSV3d	rs80338852
GWAS Ctlg	rs80338852

Max Magnitude

0

ClinVar
Risk	rs80338852(A;A)
Alt	rs80338852(A;A)
Reference	Rs80338852(T;T)
Significance	Pathogenic
Disease	Peters plus syndrome
Variation	info
Gene	B3GLCT
CLNDBN	Peters plus syndrome
Reversed	0
HGVS	NC_000013.10:g.31891736T>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000021077.1,