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rs111787668

From SNPedia

Orientationplus
Stabilizedplus
Make rs111787668(A;A)
Make rs111787668(A;C)
Make rs111787668(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position111873230
GeneFYN, LOC102724646
is asnp
is mentioned by
dbSNPrs111787668
dbSNP (old)rs111787668
ClinGenrs111787668
ebirs111787668
HLIrs111787668
Exacrs111787668
Gnomadrs111787668
Varsomers111787668
Maprs111787668
PheGenIrs111787668
Biobankrs111787668
1000 genomesrs111787668
hgdprs111787668
ensemblrs111787668
gopubmedrs111787668
geneviewrs111787668
scholarrs111787668
googlers111787668
pharmgkbrs111787668
gwascentralrs111787668
openSNPrs111787668
23andMers111787668
23andMe allrs111787668
SNP Nexus

SNPshotrs111787668
SNPdbers111787668
MSV3drs111787668
GWAS Ctlgrs111787668
Max Magnitude

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