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rs6916861

From SNPedia

Orientationplus
Stabilizedplus
Make rs6916861(A;A)
Make rs6916861(A;C)
Make rs6916861(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position111661054
GeneFYN
is asnp
is mentioned by
dbSNPrs6916861
ebirs6916861
HLIrs6916861
Exacrs6916861
Varsomers6916861
Maprs6916861
PheGenIrs6916861
hapmaprs6916861
1000 genomesrs6916861
hgdprs6916861
ensemblrs6916861
gopubmedrs6916861
geneviewrs6916861
scholarrs6916861
googlers6916861
pharmgkbrs6916861
gwascentralrs6916861
openSNPrs6916861
23andMers6916861
23andMe allrs6916861
SNP Nexus

SNPshotrs6916861
SNPdbers6916861
MSV3drs6916861
GWAS Ctlgrs6916861
GMAF0.219
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 19468241] Functional impact of endotoxin receptor CD14 polymorphisms on transcriptional activity


[PMID 24852829] The association of single nucleotide polymorphism of the Fyn gene with sporadic Alzheimer's disease in the Chinese Han population