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: rs121908501
rs121908501
STAT5B
2 0.925 0.240 17 42210189 missense variant C/G snv 0.800 1.000 3 2003 2012
dbSNP: rs761761205
rs761761205
STAT5B
1 1.000 0.120 17 42218218 frameshift variant G/-;GG delins 0.700 1.000 1 2006 2006
dbSNP: rs121908502
rs121908502
STAT5B
1 1.000 0.120 17 42223478 stop gained G/A snv 0.700 0
dbSNP: rs1555548678
rs1555548678
STAT5B
7 0.925 0.160 17 42216054 missense variant G/A snv 0.700 0
dbSNP: rs1555548680
rs1555548680
STAT5B
5 1.000 0.120 17 42216066 missense variant T/C snv 0.700 0
dbSNP: rs1555549674
rs1555549674
STAT5B
6 0.882 0.240 17 42223402 missense variant T/G snv 0.700 0