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: rs142191737
rs142191737
1 1.000 0.040 1 156137679 missense variant G/A snv 2.3E-04 2.4E-04 0.700 0
dbSNP: rs59026483
rs59026483
2 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs59684335
rs59684335
3 0.882 0.120 1 156135280 frameshift variant CT/- delins 0.700 0