Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7599488
rs7599488
BCL11A
0.925 0.120 2 60491212 intron variant C/T snv 0.42
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.800 1.000 1 2011 2011
dbSNP: rs7599488
rs7599488
BCL11A
0.925 0.120 2 60491212 intron variant C/T snv 0.42
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2015 2019
dbSNP: rs7599488
rs7599488
BCL11A
0.925 0.120 2 60491212 intron variant C/T snv 0.42
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2019
dbSNP: rs7599488
rs7599488
BCL11A
0.925 0.120 2 60491212 intron variant C/T snv 0.42
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.700 1.000 1 2011 2011