| HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
| RMRP |
|
RNA component of mitochondrial RNA processing endoribonuclease
|
|
|
0.519 |
0.731 |
| RNU4ATAC |
|
RNA, U4atac small nuclear (U12-dependent splicing)
|
|
|
0.556 |
0.808 |
| RN7SL263P |
|
RNA, 7SL, cytoplasmic 263, pseudogene
|
|
|
0.496 |
0.808 |
| TRNS1 |
|
tRNA
|
|
|
0.555 |
0.808 |
| MIR137 |
|
microRNA 137
|
|
|
0.513 |
0.846 |
| XIST |
|
X inactive specific transcript
|
|
|
0.522 |
0.808 |
| H3P8 |
|
H3 histone pseudogene 8
|
|
|
0.544 |
0.808 |
| MIR98 |
|
microRNA 98
|
|
|
0.565 |
0.731 |
| RSS |
|
Russell Silver syndrome
|
|
|
0.578 |
0.692 |
| PSS |
|
Potocki-Shaffer syndrome
|
|
|
0.608 |
0.654 |
| HYMAI |
|
hydatidiform mole associated and imprinted
|
|
|
0.670 |
0.538 |
| TRNN |
|
tRNA
|
|
|
0.682 |
0.577 |
| DNAJB1P1 |
|
DnaJ heat shock protein family (Hsp40) member B1 pseudogene 1
|
|
|
0.650 |
0.654 |
| FRAXA |
|
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
|
|
|
0.641 |
0.462 |
| FRAXE |
|
fragile site, folic acid type, rare, fra(X)(q28) E
|
|
|
0.636 |
0.462 |
| HCA1 |
|
Hypercalciuria, absorptive, 1
|
|
|
0.633 |
0.654 |
| TRD |
|
T cell receptor delta locus
|
|
|
0.650 |
0.692 |
| AMCN |
|
arthrogryposis multiplex congenita, neurogenic
|
|
|
0.682 |
0.615 |
| DCR |
|
Down syndrome chromosome region
|
|
|
0.674 |
0.538 |
| FMR1-IT1 |
|
FMR1 intronic transcript 1
|
|
|
0.716 |
0.385 |
| DEL11P13 |
|
Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
|
|
|
0.716 |
0.538 |
| CMD1B |
|
cardiomyopathy, dilated 1B (autosomal dominant)
|
|
|
0.722 |
0.500 |
| PTLS |
|
Potocki-Lupski syndrome
|
|
|
0.780 |
0.308 |
| MBS1 |
|
Moebius syndrome 1
|
|
|
0.805 |
0.308 |