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: rs121909182
rs121909182
1 1.000 0.040 16 2326027 missense variant A/G snv 0.800 1.000 1 2004 2004
dbSNP: rs121909183
rs121909183
1 1.000 0.040 16 2278348 missense variant A/G snv 0.800 1.000 1 2004 2004
dbSNP: rs121909184
rs121909184
1 1.000 0.040 16 2299442 missense variant T/C snv 0.800 1.000 1 2004 2004
dbSNP: rs28936691
rs28936691
1 1.000 0.040 16 2278016 missense variant T/G snv 0.800 1.000 1 2004 2004
dbSNP: rs149989682
rs149989682
10 0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 0.700 1.000 10 2005 2018
dbSNP: rs121909181
rs121909181
1 1.000 0.040 16 2285499 stop gained C/T snv 1.4E-05 0.700 0
dbSNP: rs1567335355
rs1567335355
1 1.000 0.040 16 2277878 splice donor variant C/T snv 0.700 0
dbSNP: rs775903641
rs775903641
1 1.000 0.040 16 2319633 frameshift variant TGTAG/- delins 7.0E-06 0.700 0