Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933990
RLBP1
0.851 0.080 15 89210794 missense variant G/A;C snv 8.6E-05; 4.8E-06 3
rs137853291
RLBP1
0.851 0.080 15 89211750 missense variant A/T snv 4.4E-05 2.8E-05 2
rs1567124404
RLBP1
0.925 0.080 15 89218627 frameshift variant T/- delins 2