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: rs387906549
rs387906549
FTH1 ; LOC399900
1 1.000 0.040 11 61967589 5 prime UTR variant T/A snv 0.700 0
dbSNP: rs1057521155
rs1057521155
SLC40A1
1 1.000 0.040 2 189575169 missense variant C/G snv 0.010 1.000 1 2006 2006
dbSNP: rs1221576286
rs1221576286
HFE ; LOC108783645
1 1.000 0.040 6 26092949 missense variant T/C snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs1318067141
rs1318067141
HFE ; LOC108783645
1 1.000 0.040 6 26092955 missense variant T/C snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs759271778
rs759271778
SLC40A1
1 1.000 0.040 2 189565575 missense variant A/G snv 7.2E-05 4.2E-05 0.010 1.000 1 2006 2006