Gene: TMEM258 ×
Source: GWASCAT ×
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: rs174529
rs174529
MYRF ; TMEM258
6 11 61776489 intron variant T/C snv 0.34 0.700 1.000 2 2018 2019
dbSNP: rs174533
rs174533
MYRF ; TMEM258
17 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 0.700 1.000 2 2017 2019