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: rs10845988
rs10845988
1 12 14368248 intron variant T/C snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs11055980
rs11055980
2 1.000 0.040 12 14458588 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs4764094
rs4764094
1 12 14490783 intron variant T/G snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs7313259
rs7313259
1 12 14475839 intron variant C/T snv 0.47 0.42 0.700 1.000 1 2017 2017