Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs1408080623
PGR ; PGR-AS1
0.851 0.080 11 101128058 missense variant G/A snv 5
rs750042441
PGR ; PGR-AS1
0.827 0.160 11 101128367 missense variant G/A;C snv 6.1E-05; 4.3E-06 5
rs776880789
PGR ; PGR-AS1
0.925 0.080 11 101128241 missense variant G/C;T snv 4.7E-06; 4.7E-06 4
rs1293387481
PGR
0.925 0.080 11 101062537 missense variant G/A snv 4.0E-06 7.0E-06 3
rs500760
PGR
0.882 0.120 11 101039260 synonymous variant T/C snv 0.24 0.29 3
rs761872690
PGR ; PGR-AS1
0.925 0.080 11 101128246 synonymous variant G/A snv 2.8E-05 3
rs1042839
PGR
0.925 0.080 11 101051471 synonymous variant G/A snv 0.13 0.11 2
rs10895054
PGR
0.925 0.080 11 101039579 intron variant A/T snv 0.11 2
rs590688
PGR
0.925 0.080 11 101105243 intron variant C/G snv 0.47 2
rs3740753
PGR-AS1 ; PGR
0.925 0.080 11 101128040 missense variant C/G snv 0.13 0.12 2
rs376101426
PGR-AS1 ; PGR
0.925 0.080 11 101128556 missense variant A/G snv 1.4E-05 2.8E-05 2
rs757679709
PGR-AS1 ; PGR
0.925 0.080 11 101129045 missense variant G/A;C snv 3.0E-05 2
rs772873062
PGR-AS1 ; PGR
0.925 0.080 11 101128998 missense variant A/G snv 4.8E-06 2
rs11571149
PGR ; PGR-AS1
0.925 0.080 11 101127937 missense variant G/T snv 2
rs1312187959
PGR ; PGR-AS1
0.925 0.080 11 101128554 missense variant C/T snv 1.4E-05 7.0E-06 2
rs518162
PGR ; PGR-AS1
0.925 0.080 11 101129770 5 prime UTR variant A/G snv 0.86 2
rs775092033
PGR ; PGR-AS1
0.925 0.080 11 101127471 missense variant G/C snv 2