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: rs137853101
rs137853101
HADH ; LOC107986298
1 1.000 0.080 4 107990050 missense variant G/A snv 0.700 0
dbSNP: rs137853102
rs137853102
HADH
1 1.000 0.080 4 108009797 missense variant C/A;T snv 8.0E-06; 4.0E-06 0.700 0
dbSNP: rs146036912
rs146036912
HADH
2 0.925 0.080 4 108027727 missense variant T/C snv 6.8E-05 9.8E-05 0.700 0