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: rs2021722
rs2021722
5 0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 0.800 1.000 2 2011 2013
dbSNP: rs2523722
rs2523722
1 1.000 0.040 6 30197496 intron variant C/T snv 0.23 0.800 1.000 1 2012 2013
dbSNP: rs116408368
rs116408368
2 1.000 0.040 6 30202733 intron variant T/C snv 0.700 1.000 2 2017 2019