. Author manuscript; available in PMC: 2017 Jan 1.

Published in final edited form as: Ann Hum Genet. 2015 Nov 27;80(1):20–31. doi: 10.1111/ahg.12139

Table 2.

Three SNPs identified by using the LRMW method, indicating a possible joint association with CHDs.

SNP, Maternal/Fetal	Gene	Ch.	Position	Allele¹	MAF²	Call Rate	Genotype Group	AUC
rs625879, Fetal	BHMT2	5	79085866	A/C	42.6%	99.0%	{CC} Vs {AA or AC}	0.54
rs2169650, Maternal	GSTP1	11	67596446	A/G	5.12%	92.5%	{GG} Vs {AA or AG}	0.58
rs8177441, Maternal	GPX3	5	151026433	C/G	21.6%	94.3%	{GG} Vs {CC or CG}	0.60

minor allele is bolded.

minor allele frequency