Source: ALL
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: rs10887800
rs10887800
RNLS ; LOC101929727
11 0.790 0.280 10 88316086 intron variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs2351791
rs2351791
ATP10D
2 0.925 0.080 4 47580370 intron variant A/C;T snv 0.76 0.010 1.000 1 2013 2013
dbSNP: rs3102735
rs3102735
TNFRSF11B ; COLEC10
12 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017