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: rs10008637
rs10008637
4 76492991 intron variant T/A;C snv 0.35
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs1010553
rs1010553
1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs10168349
rs10168349
2 46133768 intron variant G/C snv 0.36
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 3 2009 2018
dbSNP: rs10224002
rs10224002
0.925 0.080 7 151717955 intron variant A/G snv 0.31
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 1 2009 2009
dbSNP: rs10224210
rs10224210
1.000 0.040 7 151716108 intron variant T/C snv 0.21
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 2 2016 2017
dbSNP: rs10401969
rs10401969
0.776 0.240 19 19296909 intron variant T/C snv 0.10
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs10495928
rs10495928
2 46126027 intron variant A/G snv 0.36
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs10711289
rs10711289
3 169450583 intron variant AAA/-;A;AA;AAAA;AAAAA delins
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs10901252
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs10953299
rs10953299
7 100645788 intron variant T/C snv 0.21
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2018 2018
dbSNP: rs11039436
rs11039436
11 47866484 intergenic variant A/C;G;T snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs11065987
rs11065987
0.807 0.280 12 111634620 intergenic variant A/G snv 0.29
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 2 2009 2017
dbSNP: rs11072566
rs11072566
0.925 0.120 15 76001630 intron variant A/G snv 0.45
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2017 2017
dbSNP: rs11072567
rs11072567
15 76006403 intron variant A/G snv 0.43
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs111843364
rs111843364
16 70923707 intron variant G/A snv 3.8E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs112682076
rs112682076
1 10297748 intron variant G/C snv 5.8E-03
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs114948639
rs114948639
2 46066687 intron variant C/T snv 7.2E-03
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs115986297
rs115986297
6 2050557 intron variant A/C;G snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs11654074
rs11654074
17 59748211 intron variant A/C snv 0.40
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs11665867
rs11665867
19 40760574 intron variant A/G snv 0.13
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs11689538
rs11689538
2 121238062 intron variant G/C snv 0.11
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs11730623
rs11730623
4 69020433 upstream gene variant A/T snv 0.66
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2018 2018
dbSNP: rs11760376
rs11760376
7 134684558 intron variant A/G snv 1.9E-03
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs12310617
rs12310617
0.851 0.120 12 3060327 intergenic variant C/T snv 0.11
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016