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: rs142287570
rs142287570
GCM2
2 1.000 6 10874335 missense variant T/G snv 6.6E-04 4.9E-04 0.700 1.000 1 2016 2016
dbSNP: rs1057519581
rs1057519581
GCM2
1 1.000 6 10874765 missense variant G/C snv 0.700 0
dbSNP: rs1057519582
rs1057519582
GCM2
1 1.000 6 10874380 missense variant A/T snv 0.700 0
dbSNP: rs371918069
rs371918069
GCM2
2 1.000 6 10874372 missense variant C/T snv 5.6E-05 5.6E-05 0.700 0