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: rs4703129
rs4703129 		1 1.000 0.040 5 98553032 intergenic variant C/A snv 0.33 0.800 1.000 1 2010 2010
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 2009 2009
dbSNP: rs878960
rs878960
GABRB3
2 0.925 0.040 15 26683789 intron variant C/G;T snv 0.010 1.000 1 2011 2011