Disease: Red Blood Cell Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10910476 1 234599210 regulatory region variant C/A;T snv 2
rs11211480
TAL1
1 47227548 non coding transcript exon variant A/G snv 0.42 4
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs646179
USP1
1 62437203 5 prime UTR variant A/G;T snv 2
rs78024727 1 198580649 intergenic variant G/A snv 3.5E-02 2
rs10197140
ACOXL
2 110852366 intron variant T/C snv 0.28 3
rs112257498
SLC40A1
2 189568259 intron variant C/G;T snv 2
rs11683361
ANAPC1
2 111622982 intron variant C/G snv 0.70 2
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs2137283
MIR4432HG
2 60385322 non coding transcript exon variant C/A snv 0.30 4
rs2139376
MIR4435-2HG
2 111385836 intron variant T/C snv 0.44 2
rs2556097
LY75 ; LY75-CD302
2 159830550 intron variant C/A;T snv 2
rs2661794
SPRED2
2 65412409 intron variant C/A;T snv 2
rs4663199 2 235459395 regulatory region variant T/A snv 0.35 2
rs4669306
LOC105373411
2 8614076 intron variant G/A snv 0.51 2
rs5831579
LOC102724142
2 60402304 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC delins 3
rs60237566
ITM2C
2 230877996 intron variant T/G snv 0.21 0.25 2
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs72803397 2 62303123 intergenic variant G/A snv 0.15 2
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5