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: rs7130141
rs7130141
AMBRA1
1 1.000 0.040 11 46478324 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012