Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35514500 1.000 0.080 14 59387188 intergenic variant -/T delins 1
rs3789609
AP4B1-AS1 ; PTPN22
1.000 0.080 1 113855177 intron variant C/T snv 0.21 1
rs200931578
IGHV4-61
1.000 0.080 14 106639263 missense variant T/A;C snv 6.9E-03 0.23 1
rs201076896
IGHV4-61
1.000 0.080 14 106639254 missense variant T/G snv 1.1E-02 0.27 1
rs201691548
IGHV4-61
1.000 0.080 14 106639255 missense variant A/C;G;T snv 5.1E-06; 3.6E-05; 1.0E-02 1
rs202117805
IGHV4-61
1.000 0.080 14 106639291 missense variant G/A;C snv 2.0E-05; 0.14 1
rs202166511
IGHV4-61
1.000 0.080 14 106639264 missense variant A/C;G;T snv 1.5E-05; 8.5E-03; 1.0E-05 1
rs1217406
PTPN22 ; AP4B1-AS1
1.000 0.080 1 113850531 intron variant A/C snv 0.56 1