rs137852605, LBR

N. diseases: 1
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.
Pelger-Huet Anomaly
CUI: C0030779
Disease: Pelger-Huet Anomaly
7 1.000 0.080 1 225422087 missense variant G/A snv 7.0E-06 0.700 1.000 1 2003 2003