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rs16845607

From SNPedia

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Make rs16845607(A;A)
Make rs16845607(A;G)
Make rs16845607(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position173204478
GeneTNFSF4
is asnp
is mentioned by
dbSNPrs16845607
ebirs16845607
HLIrs16845607
Exacrs16845607
Varsomers16845607
Maprs16845607
PheGenIrs16845607
hapmaprs16845607
1000 genomesrs16845607
hgdprs16845607
ensemblrs16845607
gopubmedrs16845607
geneviewrs16845607
scholarrs16845607
googlers16845607
pharmgkbrs16845607
gwascentralrs16845607
openSNPrs16845607
23andMers16845607
23andMe allrs16845607
SNP Nexus

SNPshotrs16845607
SNPdbers16845607
MSV3drs16845607
GWAS Ctlgrs16845607
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 27556446] TNFSF4 Gene Variations Are Related to Early-Onset Autoimmune Thyroid Diseases and Hypothyroidism of Hashimoto's Thyroiditis.