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rs10800469

From SNPedia

Orientationplus
Stabilizedplus
Make rs10800469(A;A)
Make rs10800469(A;G)
Make rs10800469(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169736942
is asnp
is mentioned by
dbSNPrs10800469
ebirs10800469
HLIrs10800469
Exacrs10800469
Varsomers10800469
Maprs10800469
PheGenIrs10800469
hapmaprs10800469
1000 genomesrs10800469
hgdprs10800469
ensemblrs10800469
gopubmedrs10800469
geneviewrs10800469
scholarrs10800469
googlers10800469
pharmgkbrs10800469
gwascentralrs10800469
openSNPrs10800469
23andMers10800469
23andMe allrs10800469
SNP Nexus

SNPshotrs10800469
SNPdbers10800469
MSV3drs10800469
GWAS Ctlgrs10800469
GMAF0.4541
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23190470OA-icon.png] Association of SELE genotypes/haplotypes with sE-selectin levels in Taiwanese individuals: interactive effect of MMP9 level