Source: GWASCAT

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: rs877529
rs877529
1.000 0.160 22 39146287 intron variant G/A snv 0.43
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.810 1.000 1 2013 2014
dbSNP: rs139371
rs139371
1.000 0.160 22 39123191 intron variant T/C;G snv
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.800 1.000 1 2013 2013
dbSNP: rs1005300
rs1005300
1.000 0.120 22 39151886 intron variant C/G snv 0.68
CUI: C0268381
Disease: Primary amyloidosis
Primary amyloidosis
0.700 1.000 1 2017 2017
dbSNP: rs139380
rs139380
22 39130169 intron variant T/C snv 0.70
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs139402
rs139402
1.000 0.160 22 39150140 intron variant T/C snv 0.43
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.700 1.000 1 2016 2016
dbSNP: rs713909
rs713909
22 39136415 non coding transcript exon variant G/A;C;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs713909
rs713909
22 39136415 non coding transcript exon variant G/A;C;T snv
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016