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: rs117023642
rs117023642
LINC02153
2 8 20981609 intron variant C/G snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs11788387
rs11788387 		2 9 81855961 regulatory region variant G/T snv 0.14 0.700 1.000 1 2019 2019