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: rs3796863
rs3796863
CD38
8 0.790 0.160 4 15848363 intron variant G/T snv 0.41 0.020 1.000 2 2010 2012
dbSNP: rs141441277
rs141441277
SYTL4
5 0.882 0.120 X 100689933 missense variant G/A snv 5.6E-04 3.8E-04 0.010 1.000 1 2019 2019
dbSNP: rs6449197
rs6449197
CD38
3 0.882 0.120 4 15813299 intron variant C/T snv 0.23 0.010 1.000 1 2010 2010
dbSNP: rs779545541
rs779545541
GPHN
5 0.882 0.120 14 66965293 missense variant C/T snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs878960
rs878960
GABRB3
2 0.925 0.040 15 26683789 intron variant C/G;T snv 0.010 1.000 1 2011 2011