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: rs10818050
rs10818050
PTCSC2
2 9 97776641 intron variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs11026407
rs11026407
ANO5 ; LOC102723370
2 11 22083484 intron variant C/A snv 0.54 0.700 1.000 1 2014 2014
dbSNP: rs12126655
rs12126655
VAV3
2 1 107814198 intron variant A/G snv 0.33 0.700 1.000 1 2014 2014
dbSNP: rs2622590
rs2622590
XKR4
4 0.925 0.080 8 55445714 intron variant G/A snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs4704397
rs4704397
PDE8B
13 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.700 1.000 1 2008 2008
dbSNP: rs6683419
rs6683419
MICOS10 ; LOC105376819
2 1 19501286 intron variant G/A snv 0.52 0.700 1.000 1 2014 2014
dbSNP: rs925489
rs925489
PTCSC2
6 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.700 1.000 1 2014 2014