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: rs727502766
rs727502766
MAF ; LOC101928230
1 1.000 0.240 16 79599742 missense variant G/A snv 0.800 0
dbSNP: rs727502767
rs727502767
MAF ; LOC101928230
1 1.000 0.240 16 79599731 missense variant T/C snv 0.800 0
dbSNP: rs727502768
rs727502768
MAF ; LOC101928230
2 0.925 0.240 16 79599697 missense variant G/C snv 0.800 0
dbSNP: rs727502769
rs727502769
MAF ; LOC101928230
1 1.000 0.240 16 79599730 missense variant G/A snv 0.800 0
dbSNP: rs727502770
rs727502770
MAF ; LOC101928230
1 1.000 0.240 16 79599727 missense variant G/A;T snv 0.800 0
dbSNP: rs727502771
rs727502771
MAF ; LOC101928230
1 1.000 0.240 16 79599718 missense variant G/C snv 0.800 0
dbSNP: rs1481963503
rs1481963503
MAF ; LOC101928230
2 0.925 0.240 16 79598998 missense variant G/A snv 0.700 0