Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10215854
rs10215854
7 99439297 intron variant G/A snv 0.19
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011
dbSNP: rs10215854
rs10215854
7 99439297 intron variant G/A snv 0.19
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs13243267
rs13243267
7 99455691 intron variant G/C snv 0.12
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011
dbSNP: rs2280600
rs2280600
7 99450809 non coding transcript exon variant T/C snv 0.26 0.37
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011
dbSNP: rs34022779
rs34022779
7 99441691 intron variant T/-;TT;TTT delins
Dehydroepiandrosterone sulfate measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs883403
rs883403
7 99450355 synonymous variant T/A;C snv 4.0E-06; 0.26
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs883403
rs883403
7 99450355 synonymous variant T/A;C snv 4.0E-06; 0.26
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011