Gene: PGM1 ×
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: rs11208264
rs11208264
PGM1
1 1 63659401 intron variant T/C snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs11576729
rs11576729
PGM1
1 1 63648758 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12027168
rs12027168
PGM1
1 1 63654942 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs2269233
rs2269233
PGM1
1 1 63653675 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs2269234
rs2269234
PGM1
1 1 63653305 intron variant A/G snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs2269235
rs2269235
PGM1
1 1 63653244 intron variant A/G snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs2269238
rs2269238
PGM1
1 1 63651866 intron variant G/A;T snv 3.2E-05; 0.24 0.700 1.000 1 2011 2011
dbSNP: rs2269240
rs2269240
PGM1
1 1 63643593 intron variant T/C snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs2269241
rs2269241
PGM1
2 1.000 0.120 1 63643100 intron variant T/C snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs2269245
rs2269245
PGM1
1 1 63642222 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs2269246
rs2269246
PGM1
1 1 63641820 intron variant T/C snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs2269247
rs2269247
PGM1
1 1 63641613 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs2301054
rs2301054
PGM1
1 1 63641357 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs2749100
rs2749100
PGM1
1 1 63659308 intron variant G/T snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs3790857
rs3790857
PGM1
1 1 63646195 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs4643
rs4643
PGM1
1 1 63659768 3 prime UTR variant A/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs8294
rs8294
PGM1
1 1 63659697 3 prime UTR variant C/T snv 0.21 0.17 0.700 1.000 1 2011 2011