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: rs211234
rs211234
KL
1 1.000 0.040 13 33020990 intron variant G/A;C snv 0.010 1.000 1 2005 2005
dbSNP: rs211239
rs211239
KL
1 1.000 0.040 13 33022051 intron variant A/G;T snv 0.010 1.000 1 2005 2005