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: rs1554166294
rs1554166294
SLC35A1
1 1.000 0.080 6 87500616 missense variant G/C snv 0.700 0
dbSNP: rs1554166844
rs1554166844
SLC35A1
1 1.000 0.080 6 87508431 missense variant G/A snv 0.700 0
dbSNP: rs578205635
rs578205635
SLC35A1
1 1.000 0.080 6 87501270 missense variant C/G;T snv 4.0E-06; 2.4E-05 0.700 0