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rs59586681

From SNPedia

Orientationplus
Stabilizedplus
Make rs59586681(A;A)
Make rs59586681(A;T)
Make rs59586681(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position2239664
is asnp
is mentioned by
dbSNPrs59586681
ebirs59586681
HLIrs59586681
Exacrs59586681
Varsomers59586681
Maprs59586681
PheGenIrs59586681
hapmaprs59586681
1000 genomesrs59586681
hgdprs59586681
ensemblrs59586681
gopubmedrs59586681
geneviewrs59586681
scholarrs59586681
googlers59586681
pharmgkbrs59586681
gwascentralrs59586681
openSNPrs59586681
23andMers59586681
23andMe allrs59586681
SNP Nexus

SNPshotrs59586681
SNPdbers59586681
MSV3drs59586681
GWAS Ctlgrs59586681
Max Magnitude
GWAS snp
PMID [PMID 24403052OA-icon.png]
Trait Basal cell carcinoma
Title Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
Risk Allele T
P-val 3E-9
Odds Ratio 1.16 [1.11-1.22]