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: rs113471
rs113471
RXRG
1 1.000 0.160 1 165428878 synonymous variant T/C snv 0.17 0.22 0.010 1.000 1 2013 2013
dbSNP: rs2134095
rs2134095
RXRG
1 1.000 0.160 1 165408315 synonymous variant G/A;C snv 0.61; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs2194899
rs2194899
RXRG
2 1.000 0.160 1 165441548 intron variant A/G snv 0.51 0.010 1.000 1 2013 2013