Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.820 1.000 1 2012 2013
dbSNP: rs6759952
rs6759952
1.000 0.080 2 217406996 intron variant T/A;C snv
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.800 1.000 1 2013 2013
dbSNP: rs1351164
rs1351164
2 217407175 intron variant T/C snv 0.24
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2010 2010
dbSNP: rs16857609
rs16857609
0.925 0.080 2 217431785 intron variant C/T snv 0.28
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2013 2013
dbSNP: rs6435999
rs6435999
2 217658439 intron variant A/G snv 0.12
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2011 2011