Gene: TRIM26BP ×
Source: GWASDB ×
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: rs2844773
rs2844773
TRIM26BP ; HCG17
3 0.882 0.240 6 30239718 intron variant C/A snv 0.11 0.700 1.000 1 2007 2007