Disease: Lymphoproliferative Disorder of the Skin
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs11127
GNLY
0.925 0.160 2 85697606 missense variant C/T snv 0.39 0.31 3
rs1561285
GNLY
0.925 0.160 2 85697261 non coding transcript exon variant C/G snv 0.43 2
rs2886767
GNLY
0.925 0.160 2 85693206 intron variant T/C snv 0.29 2