Skip to main content
. 2022 Nov 2;12:18477. doi: 10.1038/s41598-022-22966-8

Table 3.

Significant SNPs associated with the phenotypes.

Traits SNP name Chr Position (bp) p-value Vg (%) MAF Other associated phenotypes Associated genes
Name Distance (bp)
RBC rs418188401 2 142,026,337 4.08 × 10–06 0.42 0.467 RDW_CV SCN7A Within
RBC rs415321135 2 142,135,301 1.30 × 10–05 0.48 0.351 SCN9A Within
HCT rs402657016 18 19,382,508 9.59 × 10–08 1.12 0.166 MCH, MCHC
HCT rs424122039 18 19,330,647 1.61 × 10–07 1.06 0.170 MCH, MCHC MYADM-like Within
MCH rs424122039 18 19,330,647 3.00 × 10–08 2.96 0.170 HCT, MCHC MYADM-like Within
MCH rs402657016 18 19,382,508 5.84 × 10–07 2.20 0.166 HCT, MCHC
MCHC rs424122039 18 19,330,647 4.83 × 10–11 2.15 0.170 HCT, MCH MYADM-like Within
MCHC rs402657016 18 19,382,508 2.07 × 10–09 1.82 0.166 HCT, MCH
MCV rs427024436 5 17,364,739 3.03 × 10–06 0.57 0.265 SIRT6, CREB3L3 Near
RDW_CV rs415321135 2 142,135,301 3.66 × 10–06 0.67 0.398 SCN9A Within
RDW_CV rs424460878 21 10,141,822 1.36 × 10–05 0.67 0.366 CCDC67 Within
RDW_CV rs409151807 2 142,204,729 1.48 × 10–05 0.68 0.349 SCN9A Within
RDW_CV rs418188401 2 142,026,337 2.20 × 10–05 0.40 0.467 RBC, HCT SCN7A Within
WBC rs423900300 19 11,192,604 1.19 × 10–06 0.74 0.302 ITGA9 Within
NEU rs419009933 20 45,260,345 8.94 × 10–07 4.35 0.097 LYM LOC101117887 Within
NEU rs422235744 13 43,611,954 1.75 × 10–05 1.57 0.275 LOC106991526 Within
LYM rs419009933 20 45,260,345 3.19 × 10–06 3.07 0.097 NEU LOC101117887 Within
NEU/LYM rs416257223 2 175,533,494 1.81 × 10–05 1.51 0.091 MGAT5 Within
EOS rs429955018 1 263,341,417 3.05 × 10–07 18.32 0.056 SLC19A1 Within
EOS rs424356478 3 112,927,310 3.32 × 10–05 1.98 0.466 NAV3 Near
BAS rs417370910 4 82,433,190 6.26 × 10–06 1.00 0.341 AMPH Within
PLT rs419857573 2 99,213,936 1.76 × 10–07 2.73 0.296 PCT LOC105608461 Within
PLT rs410481204 2 34,556,977 1.20 × 10–05 1.83 0.370 NTRK2 Within
MPV rs424459233 2 102,985,180 1.51 × 10–06 5.24 0.199 MSRA Within
PCT rs419857573 2 99,213,936 8.10 × 10–07 7.58 0.296 PLT LOC105608461 Within
PCT rs426696259 25 6,748,890 8.73 × 10–06 4.40 0.407 SLC35F3 Within

SNP position based on OAR_v4.0 assembly; Vg (%) is additive genetic variance explained by each SNP; MAF is minor allele frequency.