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: rs13293512
rs13293512 		11 0.763 0.360 9 94167461 intron variant T/C snv 0.24 0.010 1.000 1 2018 2018
dbSNP: rs16967637
rs16967637
STAT5A
2 0.925 0.040 17 42294404 intron variant C/A snv 0.30 0.010 1.000 1 2013 2013