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: rs1564526327
rs1564526327
1 10 74083453 frameshift variant T/- delins 0.700 0
dbSNP: rs121917776
rs121917776
VCL
5 0.882 0.040 10 74112086 missense variant C/T snv 9.9E-05 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs4746172
rs4746172
VCL
3 10 74096084 intron variant C/T snv 0.73 0.010 1.000 1 2015 2015
dbSNP: rs774870551
rs774870551
VCL
3 0.925 0.160 10 74070712 missense variant G/A snv 1.6E-05 7.0E-06 0.010 1.000 1 2017 2017