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: rs11002791
rs11002791
ZMIZ1-AS1
10 79040561 intron variant G/A snv 0.37
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs111544199
rs111544199
PRRG2 ; NOSIP
19 49587965 intron variant T/-;TT;TTTTTTT delins 0.39
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs111721712
rs111721712
HLA-B
6 31347630 intron variant -/T delins 0.55
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs112233623
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs112257498
rs112257498
SLC40A1
2 189568259 intron variant C/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs113125564
rs113125564
ZC3H4
19 47092874 intron variant T/C snv 2.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11326570
rs11326570
RAB11A ; DENND4A
15 65789510 intron variant AAA/-;A;AA;AAAA;AAAAA delins 0.27
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11338569
rs11338569
ANP32B
9 98001175 intron variant T/-;TT delins 0.25
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs113700287
rs113700287
THRB
3 24293020 intron variant -/GTT delins
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11428167
rs11428167 		3 196184704 intergenic variant -/T delins 0.13
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11451044
rs11451044
COPZ1
12 54322000 intron variant -/A ins 0.68
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs114948639
rs114948639
PRKCE
2 46066687 intron variant C/T snv 7.2E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
14 65020976 intron variant T/C snv 0.36
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11638511
rs11638511
LOC105370911
15 78259585 intron variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11657639
rs11657639 		17 48470102 downstream gene variant A/G snv 0.43
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11689538
rs11689538
TFCP2L1
2 121238062 intron variant G/C snv 0.11
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12448902
rs12448902
TUFM ; SH2B1
16 28859870 intron variant C/A;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12453682
rs12453682 		17 39613752 upstream gene variant C/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12623399
rs12623399
PRKCE
2 46122132 intron variant T/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13103322
rs13103322
LIN54
4 82974079 intron variant A/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13108043
rs13108043
AFF1
4 87123184 intron variant G/A snv 0.13
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1319012
rs1319012
USP49
6 41884878 intron variant T/A snv 0.94
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs138319634
rs138319634
FAM182B
20 25856855 intron variant G/T snv 0.12
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs140307022
rs140307022
CLCNKB
1 16043683 upstream gene variant -/GTCTG;TTCTG delins
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs144658219
rs144658219
CD36
7 80667649 intron variant -/ACTTGATT delins 0.34
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016