PLXNB2, plexin B2, 23654

N. diseases: 19; N. variants: 5
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: rs28394672
rs28394672 		22 50295194 intron variant A/G snv 0.36
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs28573806
rs28573806 		22 50289363 intron variant T/C snv 0.41
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs28578714
rs28578714 		22 50289492 intron variant T/C snv 0.35 0.41
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs5771118
rs5771118 		22 50275860 intron variant T/C snv 0.74 0.79
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs79966207
rs79966207 		22 50283979 missense variant T/C snv 0.12 0.12
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018