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
rs10772280
KLRC2
12 10428441 intron variant C/A;T snv 2
rs10910476 1 234599210 regulatory region variant C/A;T snv 2
rs10974716
SPATA6L ; PLPP6
9 4661574 intron variant C/G snv 0.20 2
rs11158716
RAD51B
14 68026441 intron variant G/A snv 0.17 2
rs112257498
SLC40A1
2 189568259 intron variant C/G;T snv 2
rs11338569
ANP32B
9 98001175 intron variant T/-;TT delins 0.25 2
rs11521
ATG101
12 52077375 3 prime UTR variant C/T snv 0.20 2
rs115616389 4 54323915 intergenic variant C/T snv 2.0E-02 2
rs11666770
MPND
19 4351655 intron variant G/C snv 0.22 2
rs11683361
ANAPC1
2 111622982 intron variant C/G snv 0.70 2
rs118111862
DLC1
8 13395479 intron variant T/C snv 5.4E-02 2
rs12146644 11 95759714 upstream gene variant A/G snv 0.28 2
rs12196049 6 121464945 intergenic variant A/C snv 0.18 2
rs12453682 17 39613752 upstream gene variant C/G;T snv 2
rs13165424 5 154973452 downstream gene variant A/G snv 0.24 2
rs140429100
PDAP1
7 99397842 intron variant G/A snv 1.5E-02 1.6E-02 2
rs144942726 13 51921254 non coding transcript exon variant C/G;T snv 2.3E-02 2
rs150317881
FYB1
5 39270693 non coding transcript exon variant C/T snv 1.0E-02 2
rs188778252 4 54182639 intron variant C/G;T snv 2
rs2139376
MIR4435-2HG
2 111385836 intron variant T/C snv 0.44 2
rs2224797
LMO7-AS1 ; LMO7
13 75636606 5 prime UTR variant A/C snv 0.50 2
rs2288789
MACIR
5 103264823 intron variant G/A snv 0.31 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
rs2672092 15 81578279 intron variant T/C snv 0.40 2