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: rs1347591
rs1347591
NUP93
1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs1347591
rs1347591
NUP93
1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2019 2019