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: rs17617068
rs17617068
1 5 179741096 intron variant T/C snv 0.23 0.800 1.000 1 2014 2014
dbSNP: rs3797776
rs3797776
1 5 179766597 synonymous variant C/T snv 0.24 0.22 0.700 1.000 1 2014 2014
dbSNP: rs4700838
rs4700838
1 5 179758120 intron variant A/G snv 0.22 0.700 1.000 1 2014 2014