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rs17047573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17047573(G;G)
Make rs17047573(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position68361969
GeneFAM19A1
is asnp
is mentioned by
dbSNPrs17047573
dbSNP (old)rs17047573
ClinGenrs17047573
ebirs17047573
HLIrs17047573
Exacrs17047573
Gnomadrs17047573
Varsomers17047573
Maprs17047573
PheGenIrs17047573
Biobankrs17047573
1000 genomesrs17047573
hgdprs17047573
ensemblrs17047573
gopubmedrs17047573
geneviewrs17047573
scholarrs17047573
googlers17047573
pharmgkbrs17047573
gwascentralrs17047573
openSNPrs17047573
23andMers17047573
23andMe allrs17047573
SNP Nexus

SNPshotrs17047573
SNPdbers17047573
MSV3drs17047573
GWAS Ctlgrs17047573
GMAF0.0854
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 20664687OA-icon.png] Single-nucleotide polymorphisms in chromosome 3p14.1- 3p14.2 are associated with susceptibility of type 2 diabetes with cataract