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: rs10877969
rs10877969
6 0.882 0.120 12 63153459 intron variant T/C snv 0.26 0.010 1.000 1 2010 2010
dbSNP: rs3759292
rs3759292
1 1.000 0.040 12 63153533 intron variant A/G snv 2.4E-02 0.010 1.000 1 2010 2010
dbSNP: rs7294536
rs7294536
2 0.925 0.040 12 63154312 upstream gene variant T/C snv 0.26 0.010 1.000 1 2010 2010