Gene: HPSE2 ×
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: rs650527
rs650527
HPSE2
1 1.000 0.040 10 98553806 intron variant C/T snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs657442
rs657442
HPSE2
1 1.000 0.040 10 98567668 intron variant A/C snv 0.84 0.700 1.000 1 2017 2017
dbSNP: rs660426
rs660426
HPSE2
1 1.000 0.040 10 98560374 intron variant C/T snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs7907389
rs7907389
HPSE2
1 1.000 0.040 10 98554582 intron variant G/A snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs898892
rs898892
HPSE2
1 1.000 0.040 10 98533943 intron variant T/C;G snv 0.700 1.000 1 2017 2017