Source: GWASDB ×
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: rs1464510
rs1464510
LPP
7 0.807 0.280 3 188394766 intron variant C/A;T snv 0.810 1.000 3 2010 2015
dbSNP: rs13076312
rs13076312
LPP
2 1.000 0.040 3 188371466 intron variant C/T snv 0.44 0.800 1.000 1 2010 2016
dbSNP: rs9851967
rs9851967
LPP
2 1.000 0.040 3 188369840 intron variant C/T snv 0.35 0.800 1.000 1 2013 2013
dbSNP: rs13091753
rs13091753
LPP
2 1.000 0.040 3 188396801 intron variant G/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs1559810
rs1559810
LPP
2 1.000 0.040 3 188406566 intron variant C/A snv 0.36 0.700 1.000 1 2010 2010