PMID: 22794791

Exploring the interaction between SNP genotype and postmenopausal hormone therapy effects on stroke risk.

Genome medicine
Y Huang, DG Ballinger, R Stokowski, E Beilharz, JG Robinson, S Liu, RD Robinson, VW Henderson, JE Rossouw, RL Prentice
2012

10 variants were identified in this publication


Variant ID Gene cDNA Protein Consequence Exon Intron
1-55527323-G-A PCSK9 c.1863+94G>A - IntronicSNV - 11/11
1-161192793-C-G APOA2 c.100G>C p.Val34Leu Missense 3/4 -
2-161336342-G-A RBMS1 c.75+13458C>T - IntronicSNV - 1/13
6-6288242-A-G F13A1 c.319+17342T>C - IntronicSNV - 3/14
1-55524842-G-A PCSK9 c.1504-317G>A - IntronicSNV - 9/11
6-6286298-G-A F13A1 c.320-19256C>T - IntronicSNV - 3/14
6-6288242-A-T F13A1 c.319+17342T>A - IntronicSNV - 3/14
6-6251120-T-A F13A1 c.614A>T p.Tyr205Phe Missense 5/15 -
6-6318795-C-T F13A1 c.103G>A p.Val35Met Missense 2/15 -
6-6318795-C-A F13A1 c.103G>T p.Val35Leu Missense 2/15 -