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: rs121434580
rs121434580
GABRD
2 0.925 0.080 1 2027636 missense variant A/C snv 0.700 1.000 1 2004 2004
dbSNP: rs139300921
rs139300921
GABRD
1 1.000 1 2028259 missense variant C/T snv 9.3E-04 8.1E-04 0.700 1.000 1 2004 2004