NCL, nucleolin, 4691

N. diseases: 167; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10202701
rs10202701
2 231463970 5 prime UTR variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs6737291
rs6737291
2 231464848 intron variant T/C snv 0.52
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019