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: rs121908650
rs121908650
WNT4
1 1.000 0.160 1 22120459 missense variant T/C snv 0.800 1.000 3 2004 2008
dbSNP: rs121908653
rs121908653
WNT4 ; LOC105376845
2 0.925 0.200 1 22142888 missense variant A/G snv 0.800 1.000 3 2004 2008
dbSNP: rs121908652
rs121908652
WNT4
1 1.000 0.160 1 22129682 missense variant G/A snv 4.0E-06 1.4E-05 0.700 0