Gene: RYR2 ×
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: rs1349176732
rs1349176732
RYR2
1 1.000 0.080 1 237445485 missense variant A/T snv 0.700 1.000 14 2001 2016
dbSNP: rs1349585791
rs1349585791
RYR2
1 1.000 0.080 1 237784148 missense variant G/A snv 0.700 1.000 14 2001 2016
dbSNP: rs1359163728
rs1359163728
RYR2
1 1.000 0.080 1 237793903 missense variant G/C snv 0.700 1.000 14 2001 2016
dbSNP: rs1456929288
rs1456929288
RYR2
1 1.000 0.080 1 237640988 missense variant G/A snv 0.700 1.000 14 2001 2016
dbSNP: rs1457271141
rs1457271141
RYR2
1 1.000 0.080 1 237791448 missense variant T/G snv 0.700 1.000 14 2001 2016
dbSNP: rs371121679
rs371121679
RYR2
1 1.000 0.080 1 237445471 missense variant G/A;T snv 8.0E-06 0.700 1.000 14 2001 2016
dbSNP: rs769219555
rs769219555
RYR2
2 0.925 0.120 1 237648612 missense variant C/T snv 4.2E-05 8.4E-05 0.700 1.000 14 2001 2016
dbSNP: rs794728747
rs794728747
RYR2
1 1.000 0.080 1 237639019 missense variant G/T snv 0.700 1.000 14 2001 2016
dbSNP: rs886039172
rs886039172
RYR2
1 1.000 0.080 1 237832591 missense variant G/A;C snv 0.700 1.000 14 2001 2016
dbSNP: rs397516539
rs397516539
RYR2
1 1.000 0.080 1 237377365 missense variant G/A;T snv 0.700 1.000 6 2006 2013
dbSNP: rs794728804
rs794728804
RYR2
1 1.000 0.080 1 237808913 missense variant G/A snv 0.700 1.000 5 2002 2015
dbSNP: rs1060500142
rs1060500142
RYR2
1 1.000 0.080 1 237330939 missense variant C/T snv 4.0E-06 0.700 1.000 3 2005 2012
dbSNP: rs794728754
rs794728754
RYR2
1 1.000 0.080 1 237640941 missense variant C/T snv 0.700 1.000 3 2010 2017
dbSNP: rs794728811
rs794728811
RYR2
2 0.925 0.080 1 237832619 missense variant G/A snv 0.700 1.000 3 2003 2005
dbSNP: rs1553339086
rs1553339086
RYR2
1 1.000 0.080 1 237819192 missense variant G/T snv 0.700 1.000 1 2009 2009
dbSNP: rs1553426678
rs1553426678
RYR2
1 1.000 0.080 1 237377374 missense variant G/A snv 0.700 1.000 1 2009 2009
dbSNP: rs1060500137
rs1060500137
RYR2
1 1.000 0.080 1 237772077 missense variant G/A snv 0.700 0
dbSNP: rs1188352725
rs1188352725
RYR2
1 1.000 0.080 1 237798091 missense variant G/C snv 0.700 0
dbSNP: rs1234963411
rs1234963411
RYR2
1 1.000 0.080 1 237784188 missense variant A/C snv 0.700 0
dbSNP: rs1239093704
rs1239093704
RYR2
1 1.000 0.080 1 237759849 missense variant G/T snv 4.0E-06 0.700 0
dbSNP: rs1242723821
rs1242723821
RYR2
1 1.000 0.080 1 237828429 missense variant T/C snv 0.700 0
dbSNP: rs1323621379
rs1323621379
RYR2
1 1.000 0.080 1 237791464 missense variant G/A snv 0.700 0
dbSNP: rs1363298408
rs1363298408
RYR2
1 1.000 0.080 1 237819144 missense variant A/G snv 0.700 0
dbSNP: rs1385881911
rs1385881911
RYR2
1 1.000 0.080 1 237784083 missense variant G/C snv 0.700 0
dbSNP: rs1472508624
rs1472508624
RYR2
1 1.000 0.080 1 237759782 missense variant C/T snv 0.700 0