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: rs387906738
rs387906738
DYNC1H1
3 0.882 0.080 14 101980506 missense variant A/G snv 0.800 1.000 3 2011 2015
dbSNP: rs587780564
rs587780564
DYNC1H1
5 0.882 0.080 14 101986017 missense variant C/T snv 0.800 1.000 3 2011 2015
dbSNP: rs1555410941
rs1555410941
DYNC1H1
1 1.000 14 102027712 missense variant G/A snv 0.700 1.000 3 2011 2015
dbSNP: rs1057518083
rs1057518083
DYNC1H1
21 0.851 0.120 14 101986552 missense variant C/T snv 0.700 1.000 2 2016 2017
dbSNP: rs794727634
rs794727634
DYNC1H1
2 0.925 0.040 14 101979952 missense variant G/A snv 0.700 1.000 1 2015 2015
dbSNP: rs1057518287
rs1057518287
DYNC1H1
3 0.882 0.080 14 102008245 missense variant G/A;T snv 0.700 0
dbSNP: rs1567019064
rs1567019064
DYNC1H1
1 1.000 14 102033145 missense variant T/C snv 0.700 0