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: rs1947988
rs1947988
1 10 105187248 intron variant C/T snv 0.24 0.700 1.000 2 2017 2019
dbSNP: rs11192193
rs11192193
2 1.000 0.040 10 104809495 intron variant A/G snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs1484246
rs1484246
1 10 105201646 intron variant G/A snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs3896224
rs3896224
1 10 104708095 intron variant A/C;G snv 0.36 0.700 1.000 1 2018 2018