Gene: PTCSC2 ×
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: rs10739496
rs10739496
PTCSC2
1 9 97790277 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10759944
rs10759944
PTCSC2
4 0.925 0.080 9 97794690 intron variant A/G snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs10818090
rs10818090
PTCSC2
1 9 97799204 intron variant C/T snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs10983700
rs10983700
PTCSC2
2 1.000 0.080 9 97775173 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10983701
rs10983701
PTCSC2
1 9 97775295 intron variant G/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs10983761
rs10983761
PTCSC2
1 9 97791675 intron variant A/C;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1443438
rs1443438
PTCSC2
8 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1561962
rs1561962
PTCSC2
1 9 97783937 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1588635
rs1588635
PTCSC2
2 1.000 0.080 9 97775520 intron variant A/C snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs1877431
rs1877431
PTCSC2
1 9 97771865 intron variant A/G snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs1912995
rs1912995
PTCSC2
1 9 97768617 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4743130
rs4743130
PTCSC2
1 9 97783758 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7021576
rs7021576
PTCSC2
1 9 97778259 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7027030
rs7027030
PTCSC2
1 9 97788173 intron variant A/C snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs7028661
rs7028661
PTCSC2
4 0.882 0.080 9 97776188 intron variant A/G snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs7030241
rs7030241
PTCSC2
1 9 97788093 intron variant T/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs7030256
rs7030256
PTCSC2
1 9 97772921 intron variant C/G snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs7030280
rs7030280
PTCSC2
2 1.000 0.080 9 97772985 intron variant C/T snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs7045465
rs7045465
PTCSC2
1 9 97772541 intron variant A/T snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs7850258
rs7850258
PTCSC2
6 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs7864322
rs7864322
PTCSC2
1 9 97786652 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs925488
rs925488
PTCSC2
2 1.000 0.040 9 97784109 intron variant G/A snv 0.71 0.700 1.000 1 2012 2012
dbSNP: rs925489
rs925489
PTCSC2
6 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.700 1.000 1 2012 2012
dbSNP: rs965513
rs965513
PTCSC2
15 0.742 0.200 9 97793827 intron variant A/G;T snv 0.700 1.000 1 2012 2012