rs9542236

Orientation

plus

Stabilized

plus

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

Make rs9542236(C;C)

Make rs9542236(C;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

31245188

Gene

B3GLCT

is a	snp
is	mentioned by
dbSNP	rs9542236
dbSNP (classic)	rs9542236
ClinGen	rs9542236
ebi	rs9542236
HLI	rs9542236
Exac	rs9542236
Gnomad	rs9542236
Varsome	rs9542236
LitVar	rs9542236
Map	rs9542236
PheGenI	rs9542236
Biobank	rs9542236
1000 genomes	rs9542236
hgdp	rs9542236
ensembl	rs9542236
geneview	rs9542236
scholar	rs9542236
google	rs9542236
pharmgkb	rs9542236
gwascentral	rs9542236
openSNP	rs9542236
23andMe	rs9542236
SNPshot	rs9542236
SNPdbe	rs9542236
MSV3d	rs9542236
GWAS Ctlg	rs9542236

GMAF

0.2429

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23455636]
Trait	Age-related macular degeneration
Title	Seven new loci associated with age-related macular degeneration.
Risk Allele	C
P-val	2E-8
Odds Ratio	1.10 [1.07-1.14]

[PMID 23868022] RAD51 gene is associated with advanced age-related macular degeneration in Chinese population

ClinVar
Risk	rs9542236(C;C)
Alt	rs9542236(C;C)
Reference	Rs9542236(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	B3GLCT
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.31819325T>C
CLNSRC
CLNACC	RCV000190310.1,