Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1168788250
rs1168788250
GLS
2 190881139 missense variant G/C snv 6.2E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs1376666756
rs1376666756
GLS
2 190881136 frameshift variant C/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs867637
rs867637
GLS ; STAT1
1.000 0.080 2 190961656 intron variant A/G;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs935566047
rs935566047
GLS
2 190881277 missense variant G/C snv 7.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017