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: rs11191560
rs11191560
NT5C2
2 10 103109281 intron variant T/C snv 8.4E-02 0.700 1.000 3 2015 2018
dbSNP: rs11191580
rs11191580
NT5C2
13 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 0.700 1.000 2 2014 2015