Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13240464
rs13240464
2 1.000 0.040 7 111258859 intron variant T/C snv 0.34 0.700 1.000 4 2014 2019
dbSNP: rs214467
rs214467
1 1.000 0.040 7 111218212 intron variant G/A;C snv 0.700 1.000 2 2017 2019
dbSNP: rs12532143
rs12532143
2 1.000 0.040 7 111385892 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs12705761
rs12705761
1 1.000 0.040 7 111336208 intron variant G/C snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs17439799
rs17439799
1 1.000 0.040 7 111101521 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs38752
rs38752
1 1.000 0.040 7 111438856 intron variant T/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs73201076
rs73201076
1 1.000 0.040 7 111135343 intron variant T/C snv 8.8E-02 0.700 1.000 1 2015 2015