Common variants in LAMC1 confer risk for pelvic organ prolapse in Chinese population

Hereditas

Table 2 10 SNPs that were selected for genotyping

SNP	Position^a	Alleles	Function	Exonic Function	AA Change
rs20558	183,125,412	T > C	exonic	missense	LAMC1:NM_002293:exon15:c.T2663C:p.L888P
rs20563	183,116,620	A > G	exonic	missense	LAMC1:NM_002293:exon7:c.A1372G:p.I458V
rs10911193	183,021,513	C > T	2 KB Upstream	.	.
rs6424889	183,122,661	G > C	intronic	.	.
rs10911241	183,094,001	A > G	intronic	.	.
rs3768617	183,123,365	C > T	intronic	.	.
rs12073936	183,092,755	T > G	intronic	.	.
rs729819	183,139,899	G > A	intronic	.	.
rs10911214	183,056,650	T > C	intronic	.	.
rs869133	183,100,146	G > C	intronic	.	.

SNP Single-nucleotide polymorphism, AA Amino acid, L Leucine, P Proline, I Isoleucine, V Valine
^aChromosomal positions are based on GRCh38 and all SNPs are located on Chromosome 1q25.3

ISSN: 1601-5223