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: rs2131877
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.800 1.000 1 2010 2010
dbSNP: rs60902112
rs60902112
XXYLT1
1.000 0.080 3 195080124 intron variant C/T snv 0.27
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 2 2018 2018
dbSNP: rs36082205
rs36082205
XXYLT1
3 195272939 upstream gene variant CC/- delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs57827131
rs57827131
XXYLT1
3 195192301 intron variant A/T snv 9.9E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs57827131
rs57827131
XXYLT1
3 195192301 intron variant A/T snv 9.9E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs73206626
rs73206626
XXYLT1
3 195100648 intron variant C/T snv 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7616009
rs7616009
XXYLT1
3 195161027 intron variant G/A snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs7644678
rs7644678
XXYLT1
3 195156120 intron variant G/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2131877
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2010 2010
dbSNP: rs2131877
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2010 2010
dbSNP: rs2131877
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs2131877
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2010 2010
dbSNP: rs2131877
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.010 1.000 1 2017 2017
dbSNP: rs9825174
rs9825174
XXYLT1
0.925 0.120 3 195118855 intron variant C/A;G;T snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.010 1.000 1 2018 2018
dbSNP: rs9825174
rs9825174
XXYLT1
0.925 0.120 3 195118855 intron variant C/A;G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2018 2018