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: rs118203895
rs118203895
LDHB
1 1.000 0.080 12 21642032 missense variant C/T snv 7.0E-06 0.800 1.000 8 1990 2001
dbSNP: rs118203896
rs118203896
LDHB
1 1.000 0.080 12 21643971 missense variant T/G snv 0.800 1.000 8 1990 2001
dbSNP: rs118203897
rs118203897
LDHB
1 1.000 0.080 12 21654653 missense variant T/C snv 1.2E-05 2.1E-05 0.800 1.000 8 1990 2001
dbSNP: rs267607212
rs267607212
LDHB
1 1.000 0.080 12 21635574 missense variant A/G snv 0.800 1.000 8 1990 2001
dbSNP: rs777954556
rs777954556
LDHB
1 1.000 0.080 12 21644037 missense variant G/A snv 8.0E-06 0.700 1.000 8 1990 2001