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: rs10764094
rs10764094
MALRD1
1 10 19621609 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs17773233
rs17773233
LOC105370653 ; LOC105370655
1 14 98116322 intron variant G/T snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs2225442
rs2225442
LINC02295 ; LOC105370655
1 14 98156257 intron variant A/C snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs4888416
rs4888416
CFDP1
1 16 75415278 intron variant C/G snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs698050
rs698050 		1 14 98071057 intron variant A/T snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs7152623
rs7152623
LOC105370655
1 14 98121984 intron variant G/A snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs9323989
rs9323989
LOC105370655
1 14 98121332 intron variant T/C snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs987514
rs987514
LINC02295 ; LOC105370655
1 14 98162606 intron variant C/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs10782490
rs10782490
LOC105370655
1 14 98083046 intron variant T/C snv 0.52 0.010 1.000 1 2018 2018
dbSNP: rs10811661
rs10811661 		22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.010 < 0.001 1 2009 2009
dbSNP: rs1381289
rs1381289
LOC105370655
1 14 98126027 intron variant C/T snv 0.42 0.010 1.000 1 2018 2018