Source: BEFREE

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: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0017638
Disease: Glioma
Glioma 		0.900 0.952 16 2009 2020
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81
CUI: C0017638
Disease: Glioma
Glioma 		0.820 1.000 2 2009 2018
dbSNP: rs115303435
rs115303435
TNFRSF6B ; RTEL1 ; RTEL1-TNFRSF6B
1.000 0.040 20 63694806 missense variant G/A snv 3.2E-03 1.1E-03
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2018 2018
dbSNP: rs6062302
rs6062302
RTEL1 ; RTEL1-TNFRSF6B
0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2018 2018