Table 1.
Gene | SNP Id.* | Chr.: Base Position* | SNP function | Alleles# |
---|---|---|---|---|
HSPA1L | rs2075800 | 6:31777946 | Missense | C/T |
rs2227956 | 6:31778272 | C/T | ||
rs2227955 | 6:31778077 | G/T | ||
HSPA4 | rs14355 | 5:132440285 | 3′ UTR | C/G |
HSPA4L | rs1380154 | 4:128723042 | Missense | C/T |
HSPA6 | rs1042881 | 1:161496530 | 3′ UTR | C/G |
HSPA9 | rs1042665 | 5:137902339 | Missense | C/T |
rs10117 | 5:137892170 | A/G |
Chr. = Chromosome
according to NCBI GRCh37.p10 assembly
ancestral allele in bold