Gene: PTCSC2 ×
Source: GWASDB ×
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: rs925489
rs925489
PTCSC2
5 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.800 1.000 1 2014 2014
dbSNP: rs10818050
rs10818050
PTCSC2
2 9 97776641 intron variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs7045138
rs7045138
PTCSC2
1 9 97829181 intron variant C/G;T snv 0.700 1.000 1 2013 2013