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rs1057979

From SNPedia

Orientationminus
Stabilizedminus
Make rs1057979(C;C)
Make rs1057979(C;G)
Make rs1057979(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position111873293
GeneFYN, LOC102724646, LOC102724705
is asnp
is mentioned by
dbSNPrs1057979
ebirs1057979
HLIrs1057979
Exacrs1057979
Varsomers1057979
Maprs1057979
PheGenIrs1057979
hapmaprs1057979
1000 genomesrs1057979
hgdprs1057979
ensemblrs1057979
gopubmedrs1057979
geneviewrs1057979
scholarrs1057979
googlers1057979
pharmgkbrs1057979
gwascentralrs1057979
openSNPrs1057979
23andMers1057979
23andMe allrs1057979
SNP Nexus

SNPshotrs1057979
SNPdbers1057979
MSV3drs1057979
GWAS Ctlgrs1057979
Max Magnitude

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