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: rs10194817
rs10194817
FKBP1B ; WDCP ; MFSD2B
2 24034181 intron variant A/G;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10194817
rs10194817
FKBP1B ; WDCP ; MFSD2B
2 24034181 intron variant A/G;T snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs4665652
rs4665652
MFSD2B
2 24027153 intron variant G/A snv 0.54
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs70944707
rs70944707
FKBP1B ; WDCP ; MFSD2B
2 24034575 intron variant TTTTTTT/-;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTTTTTTTT delins
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2016 2016
dbSNP: rs72781680
rs72781680
MFSD2B
2 24016058 intron variant C/T snv 0.10
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7561675
rs7561675
MFSD2B
2 24024948 intron variant A/G snv 0.73
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs75745192
rs75745192
FKBP1B ; WDCP ; MFSD2B
2 24047129 intron variant C/T snv 2.0E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs925228
rs925228
MFSD2B
2 24023809 intron variant A/G snv 0.73
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016