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: rs12883384
rs12883384
MDGA2
2 1.000 0.040 14 46934481 intron variant A/C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs4965121
rs4965121 		2 1.000 0.040 15 97975562 downstream gene variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs9491140
rs9491140
NKAIN2
2 1.000 0.040 6 124370091 intron variant C/T snv 0.39 0.700 1.000 1 2010 2010
dbSNP: rs9561329
rs9561329
GPC6
2 1.000 0.040 13 93358916 intron variant A/G snv 0.15 0.700 1.000 1 2010 2010