rs16861326

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs16861326(A;A)

Make rs16861326(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

17967993

is a	snp
is	mentioned by
dbSNP	rs16861326
dbSNP (classic)	rs16861326
ClinGen	rs16861326
ebi	rs16861326
HLI	rs16861326
Exac	rs16861326
Gnomad	rs16861326
Varsome	rs16861326
LitVar	rs16861326
Map	rs16861326
PheGenI	rs16861326
Biobank	rs16861326
1000 genomes	rs16861326
hgdp	rs16861326
ensembl	rs16861326
geneview	rs16861326
scholar	rs16861326
google	rs16861326
pharmgkb	rs16861326
gwascentral	rs16861326
openSNP	rs16861326
23andMe	rs16861326
SNPshot	rs16861326
SNPdbe	rs16861326
MSV3d	rs16861326
GWAS Ctlg	rs16861326

GMAF

0.02342

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 20932654]
Trait
Title	Genome-Wide Association Study to Identify Single Nucleotide Polymorphisms (SNPs) Associated With the Development of Erectile Dysfunction in African-American Men After Radiotherapy for Prostate Cancer
Risk Allele
P-val	0.000002
Odds Ratio	17.85 [NR]