Table 1.
11 SNPs within a group of five GRAMD genes analyzed in the present study.
Symbol | SNP rs ID | Commercial SNP ID | variation consequence | SNP in constrained element | GERP |
---|---|---|---|---|---|
GRAMD1A | / | / | / | / | / |
GRAMD1B | rs41761360 | ARS-BFGL-NGS-2713 | intron variant | no | 0.58 |
GRAMD1B | rs109709275 | ARS-BFGL-NGS-98,724 | splice region variant, splice polypyrimidine tract variant, intron variant | yes | 1.22 |
GRAMD1B | rs41763278 | ARS-BFGL-NGS-5976 | intron variant | no | -4.73 |
GRAMD1B | rs41756499 | ARS-BFGL-NGS-111,085 | intron variant | no | -4.73 |
GRAMD1B | rs41757840 | ARS-BFGL-NGS-116,109 |
downstream gene variant (GRAMD1B), intronic (ENSBTAG00000063982; lncRNA), exonic (ENSBTAG00000061947; lncRNA) |
yes | 0.05 |
GRAMD1C | rs41616212 | Hapmap44172-BTA-96,950 | intron variant | no | -0.46 |
GRAMD2A | rs109872173 | ARS-BFGL-NGS-113,726 | intron variant | no | 0.7 |
GRAMD2B | rs43504641 | ARS-BFGL-NGS-18,240 | intron variant | no | -6.03 |
GRAMD2B | rs110898337 | ARS-BFGL-NGS-44,139 | intron variant | no | -1.44 |
GRAMD4 | rs109247065 | ARS-BFGL-NGS-112,849 | intron variant | no | 0.29 |
GRAMD4 | rs109726105 | ARS-BFGL-NGS-1089 | downstream gene variant | no | 1.07 |