rs11079035, RAB5C

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.040 17 42136994 intron variant G/A snv 0.29 0.700 1.000 1 2013 2013
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 1.000 0.040 17 42136994 intron variant G/A snv 0.29 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 1.000 0.040 17 42136994 intron variant G/A snv 0.29 0.700 1.000 1 2019 2019