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rs17047586

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17047586(A;G)
Make rs17047586(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position68363724
GeneFAM19A1
is asnp
is mentioned by
dbSNPrs17047586
ebirs17047586
HLIrs17047586
Exacrs17047586
Varsomers17047586
Maprs17047586
PheGenIrs17047586
hapmaprs17047586
1000 genomesrs17047586
hgdprs17047586
ensemblrs17047586
gopubmedrs17047586
geneviewrs17047586
scholarrs17047586
googlers17047586
pharmgkbrs17047586
gwascentralrs17047586
openSNPrs17047586
23andMers17047586
23andMe allrs17047586
SNP Nexus

SNPshotrs17047586
SNPdbers17047586
MSV3drs17047586
GWAS Ctlgrs17047586
GMAF0.04775
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20664687OA-icon.png] Single-nucleotide polymorphisms in chromosome 3p14.1- 3p14.2 are associated with susceptibility of type 2 diabetes with cataract