| Gene |
SNP Id |
Upstream Sequence |
SNP |
Downstream Sequence |
Functional Significance |
References |
| ACVR1
|
rs1220134 |
CTTGAGGATCATATTACTCCAAGAGA |
A/T |
CTATCTGGTCATCAATTTTTATAAT |
Intron variant |
| |
| ACVR1
|
rs10497189 |
CCACAATATGCATCAAAATGTGTTCT |
C/T |
GGACATTAGTTATTCTTAATAAAGA |
Intron variant |
| |
| ACVR1
|
rs2033962 |
GTGCCATAGACCTTTGGAGGGAGCTC |
G/T |
GAAAGCTGAATTTCCTAATATGAAC |
Intron variant |
| |
| ADA
|
|
|
A4223C |
|
|
| |
| AKT2
|
rs3730051 |
GGTGGAGGGAAATTTCAGTGTCATCT |
A/G |
GTGCCCCTCTCCCTTGAGGCAGGCG |
Intron variant |
| |
| AKT2
|
rs8100018 |
aaaaaaaaaaaaaaaaaaaGCAGGGG |
C/G |
CGGGGACAGGGCAGGAGCCCATTCC |
Intron variant |
| |
| AMH
|
rs10407022 |
AGAAGACTTGGACTGGCCTCCAGGCA |
G/T |
CCCACAAGAGCCTCTGTGCCTGGTG |
I49S |
| |
| AMH
|
rs8112524 |
AGAAGACTTGGACTGGCCTCCAGGCA |
G/T |
CCCACAAGAGCCTCTGTGCCTGGTG |
Intron variant,upstream variant 2KB |
| |
| AMHR2
|
rs2002555 |
TTGTGGGACTTCAGAAGAGAGAAAGA |
C/T |
GTGGGCTGGACATCAAAGAAGGCCT |
-482 A>G |
| |
| AR
|
rs6152 |
TAGAAGTTCTGATAGCAGAAAAAAGA |
C/T |
GCAGGATTTCCACAGAAGAGAAACT |
Synonymous codon |
| |
