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: rs6532796
rs6532796
LOC100507053
2 1.000 0.040 4 99121091 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs687289
rs687289
ABO
15 1.000 0.120 9 133261703 intron variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs71446935
rs71446935
MCF2L
1 13 113080062 intron variant A/G snv 0.700 1.000 1 2019 2019
dbSNP: rs72873804
rs72873804 		1 18 5947039 intron variant G/C;T snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs776905
rs776905
F10
2 13 113127628 intron variant A/C snv 8.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs7935829
rs7935829
MS4A6A
3 1.000 0.080 11 60175342 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs7946992
rs7946992
MS4A6A
1 11 60177337 non coding transcript exon variant T/C snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs8176704
rs8176704
ABO
5 0.925 0.080 9 133260148 intron variant G/A snv 0.700 1.000 1 2013 2013
dbSNP: rs8176749
rs8176749
ABO
7 1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 0.700 1.000 1 2013 2013
dbSNP: rs9390459
rs9390459
STXBP5
2 6 147359223 synonymous variant A/G snv 0.53 0.55 0.700 1.000 1 2010 2010
dbSNP: rs9805933
rs9805933 		1 14 44551736 intron variant A/C snv 0.32 0.700 1.000 1 2019 2019