Gene: RNF157 ×
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: rs10512606
rs10512606
RNF157
1 17 76215127 intron variant A/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs7214563
rs7214563
RNF157
1 17 76218195 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019