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: rs10011838
rs10011838 		1.000 0.080 4 152599127 intergenic variant G/A snv 0.42
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10039206
rs10039206 		5 56692951 intergenic variant T/C snv 0.61
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10049088
rs10049088
LINC02029
3 157079859 upstream gene variant C/T snv 0.35
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10065892
rs10065892
AP3B1
5 78267439 intron variant G/A snv 0.27
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10071838
rs10071838
LMBRD2 ; MIR580
5 36147704 intron variant C/A;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10099100
rs10099100 		8 10719265 downstream gene variant G/C snv 0.32
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10132033
rs10132033
PPP1R36
14 64556852 intron variant T/C snv 0.16
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10132060
rs10132060
SLC7A8
14 23128526 intron variant C/T snv 0.13
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10159676
rs10159676 		10 50302023 downstream gene variant G/A snv 0.34
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: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10223451
rs10223451 		6 139630553 intron variant A/G snv 0.58
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs10224902
rs10224902
ANLN
7 36415868 synonymous variant T/C snv 0.13 0.12
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10254125
rs10254125
EIF2AK1
7 6027315 intron variant A/G snv 0.65
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10263707
rs10263707
PRKAG2
7 151706419 intron variant T/G snv 0.31
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs1029555
rs1029555 		7 26547477 upstream gene variant T/C snv 0.80
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10410723
rs10410723
RAB8A
19 16124498 non coding transcript exon variant C/A snv 0.19
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10410869
rs10410869 		19 57629913 upstream gene variant G/T snv 0.12
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs10414846
rs10414846
HAMP
19 35281568 intron variant C/T snv 0.21
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10424080
rs10424080 		19 18407968 TF binding site variant C/T snv 0.29
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10424619
rs10424619
USF2
19 35277334 non coding transcript exon variant A/G;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs1043897
rs1043897
GALNT2
1 230280653 3 prime UTR variant G/T snv 0.49
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10448
rs10448
CENPBD1P1
19 58581872 non coding transcript exon variant T/C snv 0.53
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10479001
rs10479001
PDLIM4 ; P4HA2
5 132272028 missense variant C/T snv 4.6E-02 7.2E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs1047912
rs1047912
DIP2B
12 50745079 3 prime UTR variant C/T snv 0.21
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019