Source: ALL
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: rs1131692232
rs1131692232
PUF60
6 0.851 0.160 8 143818426 inframe deletion GGGCAAAGG/- delins 0.700 0
dbSNP: rs1555429629
rs1555429629
RAD51
23 0.763 0.200 15 40729632 missense variant G/A snv 0.700 0
dbSNP: rs1372410554
rs1372410554
GLI1
1 1.000 0.080 12 57471334 missense variant A/G snv 3.5E-05 0.010 1.000 1 2017 2017