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: rs11652874
rs11652874
ASIC2
1 17 33643464 intron variant C/G snv 4.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs894079
rs894079
PHGDH
1 1 119721034 non coding transcript exon variant A/C;G snv 0.700 1.000 1 2016 2016