Table 3. Variants in genes linked to cardiovascular diseases.
Variants in genes linked to cardiovascular diseases found to be significantly more common in BEB samples compared to TSI samples. The (%) values denote fraction of individuals in the sample with the allele present. The p-values and % values are averaged over -mers constituting the associated sequences.
Gene | SN id | Variant type | Allele | p-value | %BEB | %TSI |
---|---|---|---|---|---|---|
APOB | rs2302515 | Missense | C | 1.30 | 29.29% | 8.37% |
APOB | rs676210 | Missense | A | 7.73 | 72.93% | 33.08% |
APOB | rs1042034 | Missense | C | 2.28 | 68.67% | 31.91% |
CYP11B2 | rs4545 | Missense | T | 1.31 | 31.33% | 0.91% |
CYP11B1 | rs4534 | Missense | T | 9.36 | 33.00% | 0.91% |
WNK4 | rs2290041 | Missense | T | 1.53 | 13.24% | 0.47% |
WNK4 | rs55781437 | Missense | T | 1.30 | 15.21% | 0.91% |
SLC12A3 | rs2289113 | Missense | T | 7.40 | 8.14% | 0.00% |
SCNN1A | rs10849447 | Missense | C | 8.67 | 62.88% | 39.92% |
ABO | - | 4 bp (CTGT) deletion | - | 1.17 | 29.15% | 10.55% |
ABO | rs8176741 | Missense | A | 2.06 | 27.70% | 8.45% |
SH2B3 | rs3184504 | Missense | C | 8.22 | 92.88% | 63.87% |
RAI1 | rs3803763 | Missense | C | 1.32 | 75.86% | 51.17% |
RAI1 | rs11649804 | Missense | A | 1.95 | 81.57% | 52.79% |