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: rs1029534
rs1029534
1 7 28149464 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs1557779
rs1557779
1 7 27955139 intron variant T/C snv 0.85 0.700 1.000 1 2019 2019
dbSNP: rs1635851
rs1635851
1 7 28148187 intron variant C/T snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs1635852
rs1635852
4 0.882 0.160 7 28149792 intron variant T/C snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs1708299
rs1708299
2 7 28150327 intron variant A/G snv 0.77 0.700 1.000 1 2010 2010
dbSNP: rs508347
rs508347
2 7 28173205 intron variant T/C snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs552707
rs552707
2 7 28165684 intron variant T/C snv 0.77 0.700 1.000 1 2014 2014
dbSNP: rs73091214
rs73091214
1 7 28160705 intron variant T/C snv 7.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs849141
rs849141
1 0.851 0.240 7 28145472 intron variant A/G snv 0.78 0.700 1.000 1 2009 2009