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: rs11977660
rs11977660
1 1.000 0.040 7 55094643 intron variant T/C snv 0.42 0.010 1.000 1 2019 2019
dbSNP: rs2072454
rs2072454
9 0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 0.010 1.000 1 2019 2019