Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018
dbSNP: rs11191593
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018
dbSNP: rs12219304
rs12219304
NT5C2
10 103171827 intron variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018