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rs2990510

From SNPedia

Orientationplus
Stabilizedplus
Make rs2990510(G;G)
Make rs2990510(G;T)
Make rs2990510(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position197051528
GeneF13B
is asnp
is mentioned by
dbSNPrs2990510
ebirs2990510
HLIrs2990510
Exacrs2990510
Varsomers2990510
Maprs2990510
PheGenIrs2990510
hapmaprs2990510
1000 genomesrs2990510
hgdprs2990510
ensemblrs2990510
gopubmedrs2990510
geneviewrs2990510
scholarrs2990510
googlers2990510
pharmgkbrs2990510
gwascentralrs2990510
openSNPrs2990510
23andMers2990510
23andMe allrs2990510
SNP Nexus

SNPshotrs2990510
SNPdbers2990510
MSV3drs2990510
GWAS Ctlgrs2990510
GMAF0.2397
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22704111OA-icon.png]
Trait
Title Pilot Genome-Wide Association Search Identifies Potential Loci for Risk of Erectile Dysfunction in Type 1 Diabetes Using the DCCT/EDIC Study Cohort.
Risk Allele G
P-val 0.000006
Odds Ratio None None


[PMID 18541031OA-icon.png] The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.