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: rs6871536
rs6871536
RAD50 ; TH2LCRR
2 0.827 0.160 5 132634182 intron variant T/C snv 0.24 0.710 1.000 3 2010 2016