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: rs1064792885
rs1064792885
TYMP ; SCO2
1 1.000 22 50525787 frameshift variant -/A delins 0.700 1.000 1 2009 2009
dbSNP: rs1556486467
rs1556486467
TYMP ; SCO2
1 1.000 22 50526089 frameshift variant -/A delins 0.700 1.000 1 2004 2004
dbSNP: rs1556486107
rs1556486107
TYMP ; SCO2
1 1.000 22 50525898 frameshift variant -/C delins 0.700 0
dbSNP: rs1064792881
rs1064792881
TYMP ; SCO2
1 1.000 22 50526393 inframe insertion -/CCGTCGTCCAGCGCCGCG delins 0.700 1.000 1 2002 2002
dbSNP: rs1064792880
rs1064792880
TYMP
1 1.000 22 50529610 frameshift variant -/G delins 0.700 1.000 1 2000 2000
dbSNP: rs1556486029
rs1556486029
TYMP ; SCO2
1 1.000 22 50525867 frameshift variant -/G delins 0.700 1.000 1 1999 1999
dbSNP: rs1471478620
rs1471478620
TYMP ; SCO2
1 1.000 22 50525910 frameshift variant -/G delins 0.700 0
dbSNP: rs786205097
rs786205097
TYMP ; SCO2
1 1.000 22 50525808 frameshift variant -/G delins 0.700 0
dbSNP: rs1064792865
rs1064792865
TYMP ; SCO2
1 1.000 22 50527716 start lost A/C snv 0.700 1.000 1 2000 2000
dbSNP: rs1064792867
rs1064792867
TYMP ; SCO2
1 1.000 22 50527611 missense variant A/C snv 0.700 1.000 1 2011 2011
dbSNP: rs121918044
rs121918044
POLG
6 0.807 0.240 15 89329055 missense variant A/C snv 5.7E-05 3.5E-05 0.700 0
dbSNP: rs1064792857
rs1064792857
TYMP
1 1.000 22 50529564 missense variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1060499532
rs1060499532
TYMP ; SCO2
1 1.000 22 50526338 missense variant A/G snv 0.700 1.000 1 2011 2011
dbSNP: rs1060499533
rs1060499533
TYMP ; SCO2
1 1.000 22 50526293 missense variant A/G snv 0.700 1.000 1 2003 2003
dbSNP: rs1064792862
rs1064792862
TYMP
1 1.000 22 50529155 missense variant A/G snv 0.700 1.000 1 2008 2008
dbSNP: rs1064792864
rs1064792864
TYMP
1 1.000 22 50528550 missense variant A/G snv 0.700 1.000 1 2000 2000
dbSNP: rs1064792866
rs1064792866
TYMP ; SCO2
1 1.000 22 50527704 missense variant A/G snv 0.700 1.000 1 2004 2004
dbSNP: rs1064792868
rs1064792868
TYMP ; SCO2
1 1.000 22 50527223 missense variant A/G snv 0.700 1.000 1 2005 2005
dbSNP: rs121913042
rs121913042
TYMP ; SCO2
1 1.000 22 50526650 missense variant A/G snv 7.0E-06 0.700 1.000 1 2005 2005
dbSNP: rs892141220
rs892141220
TYMP ; SCO2
1 1.000 22 50526467 missense variant A/G snv 0.700 1.000 1 2004 2004
dbSNP: rs1064792879
rs1064792879
TYMP ; SCO2
1 1.000 22 50525999 splice donor variant A/G;T snv 0.700 1.000 1 2003 2003
dbSNP: rs770277446
rs770277446
TYMP ; SCO2
1 1.000 22 50526244 splice donor variant A/G;T snv 0.700 1.000 1 2003 2003
dbSNP: rs797044454
rs797044454
TYMP
1 1.000 22 50528510 splice donor variant A/G;T snv 0.700 1.000 1 1999 1999
dbSNP: rs1064792891
rs1064792891
TYMP ; SCO2
1 1.000 22 50525819 inframe deletion AATGGC/- del 0.700 1.000 1 2011 2011
dbSNP: rs1556488264
rs1556488264
TYMP ; SCO2
4 0.925 0.120 22 50527165 inframe deletion AGC/- delins 0.700 0