PMID: 31241132

A Birth Cohort Study on the Genetic Modification of the Association of Prenatal Methylmercury With Child Cognitive Development.

American journal of epidemiology
J Julvez, G Davey Smith, S Ring, P Grandjean
2019-10-01

11 variants were identified in this publication


Variant ID Gene cDNA Protein Consequence Exon Intron
9-107647220-C-T ABCA1 c.161-371G>A - IntronicSNV - 3/49
6-160103084-C-T SOD2 c.*441G>A - 3-UTRSNV 5/5 -
16-56667614-C-T MT1M c.95-49C>T - IntronicSNV - 2/2
16-56667614-C-A MT1M c.95-49C>A - IntronicSNV - 2/2
16-56667614-C-G MT1M c.95-49C>G - IntronicSNV - 2/2
7-94937446-T-C PON1 c.575A>G p.Gln192Arg Missense 6/9 -
11-100933412-C-A PGR c.1978G>T p.Val660Leu Missense 4/8 -
11-100933412-C-G PGR c.1978G>C p.Val660Leu Missense 4/8 -
9-107647655-G-A ABCA1 c.161-806C>T - IntronicSNV - 3/49
9-107647655-G-T ABCA1 c.161-806C>A - IntronicSNV - 3/49
3-133484029-G-A TF c.1330+278G>A - IntronicSNV - 11/16