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: rs2288831
rs2288831
2 0.925 0.080 5 159323005 intron variant T/C snv 0.28 0.26 0.010 1.000 1 2013 2013
dbSNP: rs3212217
rs3212217
3 0.925 0.040 5 159328122 intron variant C/G snv 0.26 0.010 1.000 1 2018 2018
dbSNP: rs919766
rs919766
1 1.000 0.040 5 159320556 intron variant A/C snv 0.12 0.14 0.010 1.000 1 2013 2013