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: rs1173730
rs1173730
1 5 32763740 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs2194178
rs2194178
1 5 32717938 intron variant C/T snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs34555832
rs34555832
1 5 32777239 intron variant G/A;C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs3792752
rs3792752
1 5 32768528 intron variant A/G snv 0.31 0.700 1.000 1 2010 2010
dbSNP: rs6450922
rs6450922
1 5 32689612 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs72742734
rs72742734
1 5 32773169 intron variant A/G snv 3.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs7731703
rs7731703
1 5 32694836 intron variant C/T snv 0.31 0.700 1.000 1 2014 2014