Source: CLINVAR ×
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: rs80359818
rs80359818
SLC2A1
5 0.776 0.360 1 42930766 missense variant G/A snv 0.800 1.000 3 2002 2009
dbSNP: rs1553155986
rs1553155986
SLC2A1
5 0.827 0.280 1 42929008 missense variant C/T snv 0.800 1.000 0 1999 2018
dbSNP: rs80359825
rs80359825
SLC2A1
6 0.790 0.360 1 42929009 missense variant G/A snv 0.800 0
dbSNP: rs776095655
rs776095655
SLC2A1
7 0.827 0.160 1 42927684 missense variant C/A;T snv 4.0E-06 0.700 1.000 3 2011 2015
dbSNP: rs796053272
rs796053272
SLC2A1
5 0.827 0.360 1 42943323 splice acceptor variant T/C snv 0.700 1.000 1 2014 2014
dbSNP: rs80359826
rs80359826
SLC2A1
6 0.807 0.120 1 42929018 stop gained G/A;T snv 4.0E-06 0.700 1.000 1 2000 2000
dbSNP: rs121909740
rs121909740
SLC2A1
2 0.925 0.120 1 42929637 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs13306758
rs13306758
SLC2A1
6 0.807 0.360 1 42927148 missense variant G/A;T snv 2.8E-03 0.700 0
dbSNP: rs1553155973
rs1553155973
SLC2A1
1 1.000 0.080 1 42928964 frameshift variant CAACCCGCCA/- delins 0.700 0
dbSNP: rs1553156069
rs1553156069
SLC2A1
1 1.000 0.080 1 42929728 frameshift variant C/- del 0.700 0
dbSNP: rs1557644984
rs1557644984
SLC2A1
5 0.925 0.080 1 42927622 missense variant A/G snv 0.700 0
dbSNP: rs1557646075
rs1557646075
SLC2A1
1 1.000 0.080 1 42929923 inframe deletion TCTCGGGGC/- delins 0.700 0
dbSNP: rs1557646673
rs1557646673
SLC2A1
1 1.000 0.080 1 42930842 frameshift variant -/T delins 0.700 0
dbSNP: rs1557646867
rs1557646867
SLC2A1
5 0.827 0.360 1 42931159 frameshift variant -/T delins 0.700 0
dbSNP: rs587784390
rs587784390
SLC2A1
1 1.000 0.080 1 42943240 missense variant T/C snv 0.700 0
dbSNP: rs587784391
rs587784391
SLC2A1
1 1.000 0.080 1 42927794 frameshift variant C/- delins 0.700 0
dbSNP: rs587784393
rs587784393
SLC2A1
1 1.000 0.080 1 42943312 splice acceptor variant CGTCAGCTTC/- delins 0.700 0
dbSNP: rs587784396
rs587784396
SLC2A1
1 1.000 0.080 1 42929712 stop gained G/A snv 0.700 0
dbSNP: rs587784397
rs587784397
SLC2A1
1 1.000 0.080 1 42929613 stop gained G/A snv 0.700 0
dbSNP: rs796053248
rs796053248
SLC2A1
6 0.807 0.360 1 42929885 missense variant G/A;T snv 4.0E-06 0.700 0
dbSNP: rs80359814
rs80359814
SLC2A1
1 1.000 0.080 1 42931049 missense variant C/T snv 0.700 0
dbSNP: rs80359816
rs80359816
SLC2A1
2 0.882 0.080 1 42930765 missense variant C/A;T snv 0.700 0
dbSNP: rs80359823
rs80359823
SLC2A1
1 0.882 0.080 1 42929298 missense variant G/A snv 0.700 0
dbSNP: rs80359828
rs80359828
SLC2A1
1 1.000 0.080 1 42927173 stop gained G/T snv 0.700 0
dbSNP: rs80359829
rs80359829
SLC2A1
1 1.000 0.080 1 42927154 stop gained T/A snv 0.700 0