Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039807
TMEM231
0.776 0.480 16 75541466 non coding transcript exon variant A/G snv 4.2E-06 11
rs753709447
TMEM231
1.000 0.160 16 75555881 missense variant C/A snv 2.3E-05 2.1E-05 1