rs8135665

Orientation

plus

Stabilized

plus

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

Make rs8135665(C;T)

Make rs8135665(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

38080269

Gene	LOC105373027, SLC16A8

is a	snp
is	mentioned by
dbSNP	rs8135665
dbSNP (classic)	rs8135665
ClinGen	rs8135665
ebi	rs8135665
HLI	rs8135665
Exac	rs8135665
Gnomad	rs8135665
Varsome	rs8135665
LitVar	rs8135665
Map	rs8135665
PheGenI	rs8135665
Biobank	rs8135665
1000 genomes	rs8135665
hgdp	rs8135665
ensembl	rs8135665
geneview	rs8135665
scholar	rs8135665
google	rs8135665
pharmgkb	rs8135665
gwascentral	rs8135665
openSNP	rs8135665
23andMe	rs8135665
SNPshot	rs8135665
SNPdbe	rs8135665
MSV3d	rs8135665
GWAS Ctlg	rs8135665

GMAF

0.2236

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	T
P-val	2E-11
Odds Ratio	1.15 [1.11-1.19]

ClinVar
Risk	rs8135665(T;T)
Alt	rs8135665(T;T)
Reference	Rs8135665(C;C)
Significance	Untested
Disease	not provided
Variation	info
Gene	LOC101927119 SLC16A8
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.38476276C>T
CLNSRC
CLNACC	RCV000190316.1,