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: rs11191379
rs11191379
SFXN2
10 102722573 intron variant C/T snv 0.12
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2902548
rs2902548
SFXN2
10 102727625 intron variant C/T snv 0.18 0.20
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
dbSNP: rs7917772
rs7917772
SFXN2
10 102727686 3 prime UTR variant G/A;C snv 0.46
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs7917772
rs7917772
SFXN2
10 102727686 3 prime UTR variant G/A;C snv 0.46
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7917772
rs7917772
SFXN2
10 102727686 3 prime UTR variant G/A;C snv 0.46
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017