Gene: TMEM258 ×
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: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.700 1.000 2 2012 2013
dbSNP: rs108499
rs108499
MYRF ; TMEM258
2 11 61779765 intron variant C/T snv 0.27 0.700 1.000 2 2012 2013
dbSNP: rs174528
rs174528
MYRF ; TMEM258
5 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 2 2012 2013
dbSNP: rs174534
rs174534
MYRF ; TMEM258
3 1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 0.700 1.000 2 2012 2013
dbSNP: rs174535
rs174535
MYRF ; TMEM258
19 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 0.700 1.000 2 2012 2013
dbSNP: rs174536
rs174536
MYRF ; TMEM258
3 11 61784455 non coding transcript exon variant A/C snv 0.29 0.700 1.000 2 2012 2013
dbSNP: rs174537
rs174537
MYRF ; TMEM258
23 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 2 2012 2013
dbSNP: rs174538
rs174538
TMEM258 ; FEN1 ; MIR611
21 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 0.700 1.000 2 2012 2013
dbSNP: rs102274
rs102274
TMEM258
3 1.000 0.080 11 61790354 non coding transcript exon variant T/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs149803
rs149803
MYRF ; TMEM258
2 11 61771548 synonymous variant C/G;T snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs149804
rs149804
MYRF ; TMEM258
1 11 61771134 intron variant A/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs174529
rs174529
MYRF ; TMEM258
7 11 61776489 intron variant T/C snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs174530
rs174530
MYRF ; TMEM258
4 1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs174532
rs174532
MYRF ; TMEM258
2 11 61781402 intron variant G/A snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs174533
rs174533
MYRF ; TMEM258
18 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 0.700 1.000 1 2012 2012
dbSNP: rs17762402
rs17762402
MYRF ; TMEM258
2 11 61785729 intron variant G/A snv 4.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs2269928
rs2269928
MYRF ; TMEM258
2 11 61770057 intron variant T/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs412334
rs412334
TMEM258 ; FEN1 ; MIR611
2 11 61792789 5 prime UTR variant C/T snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs509360
rs509360
MYRF ; TMEM258
3 11 61781087 intron variant A/G snv 0.61 0.52 0.700 1.000 1 2012 2012
dbSNP: rs579383
rs579383
MYRF ; TMEM258
2 11 61769111 intron variant G/A snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs61747222
rs61747222
MYRF ; TMEM258
1 11 61781324 missense variant G/A snv 2.2E-02 2.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs61896141
rs61896141
MYRF ; TMEM258
2 11 61788567 intron variant A/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs628993
rs628993
MYRF ; TMEM258
1 11 61772219 intron variant G/A snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs650436
rs650436
MYRF ; TMEM258
2 11 61768958 intron variant C/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs740006
rs740006
TMEM258
2 11 61790396 3 prime UTR variant T/C snv 7.6E-02 0.700 1.000 1 2012 2012