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: rs17035646
rs17035646
6 1 10736490 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs34071855
rs34071855
4 1 10738432 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs35295665
rs35295665
2 1 10737371 intron variant -/C delins 0.700 1.000 1 2018 2018