OAR pos. (bp) for most significant SNP | Annotation class for the most significant variant | M-GWAS Pval | ygfw | agfw | ycfw | acfw | ysl | asl | yfd | afd | ydcv | adcv | ycuv | acuv | yss | ass | ebwr | ebcov | Flanking genesa |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Chr3:58,729,692 | Intronic | 3.21E−43 | 4.6 | 3.9 | − 10.9 | − 5.5 | − 6.7 | − 3.9 | 3.3 | 5.1 | − 3.2 | − 2.3 | − 4.2 | 6.9 | 3.5 | THNSL20 | |||
Chr25:35,305,108 | Intronic | 4.85E−40 | 5.1 | 2.9 | 6.7 | 3.3 | 4.6 | 4.6 | 4.4 | 2.8 | − 9.6 | − 6.8 | − 4.5 | − 3 | 10.4 | 8.8 | MAT1A0 | ||
Chr19:840,732 | Missense | 4.44E−30 | 4.9 | 4.1 | 2 | − 2.5 | − 2.1 | − 2.6 | EGFR0 | ||||||||||
Chr13:62,835,771 | Intergenic | 3.30E−14 | 4 | 2 | 3.8 | 4 | 3.1 | 4.7 | 3.4 | 6.2 | 4.7 | − 2.2 | − 2.5 | − 2.5 | RALY16 EIF2S271 | ||||
Chr6:37,676,407 | intergenic | 4.87E-12 | 3.9 | 6.2 | 3.6 | 5.2 | − 2.6 | − 3.1 | 3.5 | 2.1 | LCORL224 | ||||||||
Chr15:72,567,959 | intronic | 5.92E-09 | 2.9 | 6.6 | 3.8 | − 3.7 | ALX40 | ||||||||||||
Chr3:86,858,557 | Intronic | 1.29E−07 | 2 | 2.3 | 5.1 | 3.7 | − 2.7 | EIF2AK20 | |||||||||||
Chr9:82,254,047 | Intronic | 8.29E−07 | 3.8 | 3.9 | − 2.8 | − 2.1 | − 2.7 | − 2.9 | ESRP10 | ||||||||||
Chr23:43,896,965 | Upstream | 3.07E−06 | − 3.3 | − 2.9 | 5.4 | 3.4 | − 3.3 | − 2.5 | 3.6 | MC2R2.2 | |||||||||
MC5R27 | |||||||||||||||||||
Chr9:29,973,331 | Intergenic | 4.59E−06 | 3.2 | 5.2 | 3.4 | 2.8 | − 2.1 | − 2.4 | ZHX2327 | ||||||||||
HAS2970 | |||||||||||||||||||
Chr3:58,952,741 | Intergenic | 3.41E−06 | 2.8 | 4.2 | 3.4 | −2.4 | 2 | 3.9 | − 4.6 | − 2.1 | FOXI334 | ||||||||
THNSL2213 | |||||||||||||||||||
Chr1:259,689,936 | Intronic | 1.97E−06 | 2.2 | 2 | 3.1 | 3.1 | − 5.8 | − 3.9 | 2.7 | − 2.1 | bMX20 |