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rs7768046

From SNPedia

Orientationplus
Stabilizedplus
Make rs7768046(A;A)
Make rs7768046(A;G)
Make rs7768046(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position111858729
GeneFYN, LOC102724705
is asnp
is mentioned by
dbSNPrs7768046
ebirs7768046
HLIrs7768046
Exacrs7768046
Varsomers7768046
Maprs7768046
PheGenIrs7768046
hapmaprs7768046
1000 genomesrs7768046
hgdprs7768046
ensemblrs7768046
gopubmedrs7768046
geneviewrs7768046
scholarrs7768046
googlers7768046
pharmgkbrs7768046
gwascentralrs7768046
openSNPrs7768046
23andMers7768046
23andMe allrs7768046
SNP Nexus

SNPshotrs7768046
SNPdbers7768046
MSV3drs7768046
GWAS Ctlgrs7768046
Max Magnitude
? (A;A) (A;G) (G;G) 28

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