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: rs121909658
rs121909658
FSHR
8 0.776 0.200 2 48983125 missense variant G/A snv 6.9E-04 5.8E-04 0.700 0
dbSNP: rs121909659
rs121909659
FSHR
2 0.925 0.160 2 48989022 missense variant A/G;T snv 4.0E-05; 4.0E-06 0.700 0
dbSNP: rs121909660
rs121909660
FSHR
1 1.000 0.160 2 48963104 missense variant G/A snv 1.2E-05 0.700 0
dbSNP: rs121909661
rs121909661
FSHR
2 0.925 0.200 2 48963566 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs121909662
rs121909662
FSHR
1 1.000 0.160 2 48963266 missense variant G/A;T snv 4.0E-06 0.700 0
dbSNP: rs386833510
rs386833510
FSHR
1 1.000 0.160 2 48963778 missense variant G/C snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs386833511
rs386833511
FSHR
3 0.882 0.200 2 48963097 missense variant G/A snv 0.700 0
dbSNP: rs386833512
rs386833512
FSHR
1 1.000 0.160 2 48963061 missense variant G/T snv 0.700 0
dbSNP: rs386833513
rs386833513
FSHR
1 1.000 0.160 2 48963020 missense variant G/C snv 0.700 0
dbSNP: rs386833514
rs386833514
FSHR
1 1.000 0.160 2 48982918 missense variant A/C snv 0.700 0
dbSNP: rs386833515
rs386833515
FSHR
1 1.000 0.160 2 48968881 missense variant T/A;C snv 0.700 0