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rs975121

From SNPedia

Orientationplus
Stabilizedplus
Make rs975121(A;A)
Make rs975121(A;G)
Make rs975121(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position192179429
GeneFGF12
is asnp
is mentioned by
dbSNPrs975121
ebirs975121
HLIrs975121
Exacrs975121
Varsomers975121
Maprs975121
PheGenIrs975121
hapmaprs975121
1000 genomesrs975121
hgdprs975121
ensemblrs975121
gopubmedrs975121
geneviewrs975121
scholarrs975121
googlers975121
pharmgkbrs975121
gwascentralrs975121
openSNPrs975121
23andMers975121
23andMe allrs975121
SNP Nexus

SNPshotrs975121
SNPdbers975121
MSV3drs975121
GWAS Ctlgrs975121
GMAF0.2658
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21139019OA-icon.png]
Trait
Title A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum
Risk Allele
P-val 0.000007
Odds Ratio 2.1700 [1.55-3.03]