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: rs4654748
rs4654748
NBPF3
3 1.000 0.040 1 21459575 intron variant C/T snv 0.38 0.800 1.000 4 2009 2018
dbSNP: rs10056527
rs10056527
ZNF608
1 5 124740390 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1106357
rs1106357 		3 1 21490592 intergenic variant C/T snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs12118362
rs12118362
NBPF3
1 1 21445504 intron variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs12132412
rs12132412 		1 1 21493549 intergenic variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs1256335
rs1256335
ALPL
2 1 21563893 intron variant G/A snv 0.80 0.700 1.000 1 2009 2009
dbSNP: rs1697421
rs1697421 		3 1 21496799 intergenic variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs1772719
rs1772719
ALPL
1 1 21577881 3 prime UTR variant A/C snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs2267739
rs2267739
ADCYAP1R1
1 7 31097283 intron variant C/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs28789220
rs28789220
LOC102723493
1 15 66988590 intron variant G/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs4654932
rs4654932
NBPF2P
2 1 21425060 intron variant G/A;C snv 0.700 1.000 1 2013 2013