Gene: NT5C2 ×
Source: ALL
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: rs11191593
rs11191593
NT5C2
4 10 103179458 intron variant T/C snv 9.0E-02 0.700 1.000 3 2011 2018
dbSNP: rs11191580
rs11191580
NT5C2
13 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs12416331
rs12416331
NT5C2
2 1.000 0.040 10 103169157 intron variant T/A snv 8.4E-02 0.700 1.000 1 2018 2018