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: rs10953299
rs10953299
ACTL6B
7 100645788 intron variant T/C snv 0.21
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2018 2018
dbSNP: rs2075672
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2017 2017