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: rs12027135
rs12027135
3 1 25449242 intron variant A/T snv 0.50 0.800 1.000 4 2010 2019
dbSNP: rs10903129
rs10903129
4 1 25442446 intron variant A/G snv 0.58 0.700 1.000 2 2018 2019
dbSNP: rs11802413
rs11802413
1 1 25434429 intron variant C/T snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs12027110
rs12027110
1 1 25449191 intron variant A/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs139604259
rs139604259
1 1 25442718 intron variant -/A delins 0.58 0.700 1.000 1 2018 2018
dbSNP: rs9438905
rs9438905
2 1 25437686 intron variant A/G snv 0.59 0.700 1.000 1 2019 2019