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: rs1554616628
rs1554616628
2 1.000 7 76329927 missense variant G/A snv 0.800 1.000 1 2017 2017
dbSNP: rs1554616630
rs1554616630
1 1.000 7 76329934 missense variant G/C snv 0.800 1.000 1 2017 2017
dbSNP: rs1554616627
rs1554616627
1 1.000 7 76329923 missense variant T/G snv 0.700 1.000 1 2017 2017
dbSNP: rs1554618767
rs1554618767
1 1.000 7 76358765 missense variant T/G snv 0.700 1.000 1 2017 2017