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: rs137853105
rs137853105
4 0.882 0.160 17 58206479 missense variant A/C snv 5.6E-05 2.8E-05 0.700 0
dbSNP: rs1488635637
rs1488635637
6 0.827 0.360 17 58208003 splice acceptor variant T/C;G snv 7.0E-06 0.700 0
dbSNP: rs754279998
rs754279998
10 0.776 0.360 17 58208153 inframe deletion GAG/- delins 2.0E-05 1.4E-05 0.700 0
dbSNP: rs786205508
rs786205508
5 0.851 0.200 17 58208542 stop gained G/A snv 0.700 0
dbSNP: rs886039803
rs886039803
3 0.925 0.120 17 58216664 splice donor variant A/T snv 0.700 0