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: rs104894205
rs104894205
CSRP3
3 0.882 0.040 11 19188286 missense variant A/G snv 1.2E-05 5.6E-05 0.700 1.000 4 2006 2017
dbSNP: rs45550635
rs45550635
CSRP3
1 1.000 0.040 11 19192439 missense variant A/G snv 2.2E-03 2.7E-03 0.700 1.000 3 2002 2008
dbSNP: rs45552933
rs45552933
CSRP3
1 1.000 0.040 11 19188203 missense variant C/T snv 2.4E-05 2.8E-05 0.700 1.000 3 2002 2008
dbSNP: rs761507504
rs761507504
CSRP3
2 0.925 0.040 11 19185011 missense variant C/T snv 1.2E-05 7.0E-06 0.700 1.000 2 2013 2015