Association of TCN1-rs34530014 with VB12 concentration
Trait . | Study . | SNP . | CHR:POS . | N . | EA/NEA . | EAF . | BETA (SE) . | P* . |
---|---|---|---|---|---|---|---|---|
VB12 | JHS | rs34530014 | 11:59631467 | 1280 | A/AC | 0.036 | −0.817 (0.104) | 6.48 × 10−15 |
VB12 | BioVU | rs11822978 | 11:59626896 | 725 | T/C | 0.034 | −0.158 (0.038) | 3.28 × 10−5 |
VB12 | BioMe | rs11822978 | 11:59626896 | 3199 | T/C | 0.032 | −0.272 (0.037) | 2.76 × 10−13 |
Trait . | Study . | SNP . | CHR:POS . | N . | EA/NEA . | EAF . | BETA (SE) . | P* . |
---|---|---|---|---|---|---|---|---|
VB12 | JHS | rs34530014 | 11:59631467 | 1280 | A/AC | 0.036 | −0.817 (0.104) | 6.48 × 10−15 |
VB12 | BioVU | rs11822978 | 11:59626896 | 725 | T/C | 0.034 | −0.158 (0.038) | 3.28 × 10−5 |
VB12 | BioMe | rs11822978 | 11:59626896 | 3199 | T/C | 0.032 | −0.272 (0.037) | 2.76 × 10−13 |
CHR, chromosome; EA, effect allele; EAF, effect allele frequency; NEA, noneffect allele; POS, position; SE, standard error; SNP, single nucleotide polymorphism.
Genome-wide significance was predefined as P < 1.69 × 10−9 or 0.05/29 665 030 variants tested.