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: rs11191580
rs11191580
10 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 0.700 1.000 3 2017 2019
dbSNP: rs11191593
rs11191593
3 10 103179458 intron variant T/C snv 9.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs117208459
rs117208459
1 10 103126864 intron variant T/A snv 1.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs77420391
rs77420391
2 1.000 0.040 10 103186066 intron variant G/A snv 8.9E-02 0.700 1.000 1 2018 2018