rs478304

Orientation

minus

Stabilized

minus

Make rs478304(A;A)

Make rs478304(A;C)

Make rs478304(C;C)

Reference

GRCh38 38.1/142

Chromosome

11

Position

65726789

is a	snp
is	mentioned by
dbSNP	rs478304
dbSNP (classic)	rs478304
ClinGen	rs478304
ebi	rs478304
HLI	rs478304
Exac	rs478304
Gnomad	rs478304
Varsome	rs478304
LitVar	rs478304
Map	rs478304
PheGenI	rs478304
Biobank	rs478304
1000 genomes	rs478304
hgdp	rs478304
ensembl	rs478304
geneview	rs478304
scholar	rs478304
google	rs478304
pharmgkb	rs478304
gwascentral	rs478304
openSNP	rs478304
23andMe	rs478304
SNPshot	rs478304
SNPdbe	rs478304
MSV3d	rs478304
GWAS Ctlg	rs478304

Max Magnitude

0

GWAS snp
PMID	[PMID 24927181]
Trait	Acne (severe)
Title	Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
Risk Allele	T
P-val	3E-11
Odds Ratio	1.20 [1.11-1.29]