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: rs769114543
rs769114543
ALG14 ; ALG14-AS1
1 1.000 1 95064934 missense variant C/T snv 1.6E-04 1.2E-04 0.700 1.000 1 2017 2017
dbSNP: rs367570129
rs367570129
ALG14 ; LOC105378863
1 1.000 1 95027239 stop gained G/A snv 4.0E-05 4.2E-05 0.700 0
dbSNP: rs730882050
rs730882050
ALG14 ; ALG14-AS1
1 1.000 1 95064960 missense variant G/A snv 0.700 0