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rs1810636

From SNPedia

Orientationminus
Stabilizedminus
Make rs1810636(G;G)
Make rs1810636(G;T)
Make rs1810636(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position2674279
is asnp
is mentioned by
dbSNPrs1810636
ebirs1810636
HLIrs1810636
Exacrs1810636
Varsomers1810636
Maprs1810636
PheGenIrs1810636
hapmaprs1810636
1000 genomesrs1810636
hgdprs1810636
ensemblrs1810636
gopubmedrs1810636
geneviewrs1810636
scholarrs1810636
googlers1810636
pharmgkbrs1810636
gwascentralrs1810636
openSNPrs1810636
23andMers1810636
23andMe allrs1810636
SNP Nexus

SNPshotrs1810636
SNPdbers1810636
MSV3drs1810636
GWAS Ctlgrs1810636
GMAF0.3802
Max Magnitude
? (G;G) (G;T) (T;T) 28

Mentioned in retracted [PMID 20595579]


[PMID 22105264OA-icon.png] Identification of six Loci associated with pelvic organ prolapse using genome-wide association analysis