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: rs12429206
rs12429206
1 13 50871978 intron variant A/G snv 0.62 0.700 1.000 1 2017 2017
dbSNP: rs202346
rs202346
1 13 50513307 intron variant C/A snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs9596300
rs9596300
1 13 50507855 intron variant A/C;G;T snv 0.700 1.000 1 2017 2017