Source: ALL
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: rs1033069
rs1033069
SPAG16
1 1.000 0.040 2 213900484 intron variant A/G snv 0.58 0.010 1.000 1 2013 2013
dbSNP: rs11103603
rs11103603 		4 0.851 0.080 9 134449754 TF binding site variant T/C snv 0.46 0.010 1.000 1 2019 2019
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2009 2009
dbSNP: rs6776706
rs6776706
RARB
4 0.851 0.080 3 25439731 intron variant T/A snv 0.27 0.010 1.000 1 2019 2019