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Table 2 10 SNPs that were selected for genotyping

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

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