Gene: SH3TC2 ×
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: rs9687065
rs9687065
SH3TC2
2 5 149011577 intron variant A/G snv 0.17 0.700 1.000 2 2015 2017
dbSNP: rs7704297
rs7704297
SH3TC2
2 5 149010732 intron variant T/C snv 0.16 0.700 1.000 1 2017 2017