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: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs8069176
rs8069176 		4 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs8076131
rs8076131
ORMDL3
11 0.790 0.200 17 39924659 intron variant G/A;C snv 0.010 1.000 1 2018 2018