| Gene |
Chromosome |
Location |
Syndrome |
Category |
| VAMP1 | 12 | p13.31 | Spastic ataxia autosomal dominant type 01 | Ataxia spectrum | |
| VAPB | 20 | q13.32 | ALS | ALS - amyotrophic lateral sclerosis | |
| VAX1 | 10 | q26.1 | Syndromic Microphthalmia | Cleft lip / cleft palate | |
| VCAN | 5 | q14.2 | Wagner syndrome | Cataracts | |
| VCP | 9 | p13.3 | ALS | ALS - amyotrophic lateral sclerosis | |
| VDR | 12 | q13.11 | Hereditary vitamin D-resistant rickets type 2 | Alopecia | |
| VEGFA | 6 | p21.1 | microvascular complications of diabetes 1 | Diabetes | |
| VERBRAS | 3 | p21.31 | VERVERI-BRADY SYNDROME | Autism spectrum | |
| VETD | 17 | q23.2 | VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION | Autism spectrum | |
| VHL | 3 | p25.3 | Von Hippel-Lindau syndrome | Ataxia spectrum | |
| VIM | 10 | p13 | Cataract 30 multiple types (CTRCT30) | Cataracts | |
| VIPAS39 | 14 | q24.3 | Arthrogryposis renal dysfunction and cholestasis syndrome 2 (ARCS2) | Arthrogryposis spectrum | |
| VLDLR | 9 | p24.2 | VLDLR-associated cerebellar hypoplasia | Ataxia spectrum | |
| VMLDS1 | 11 | p15.4 | VAN MALDERGEM SYNDROME 1 | Autism spectrum | |
| VPS13A | 9 | q21.2 | Chorea-acanthocytosis | Panic phobia anxiety | |
| VPS13B | 8 | q22.2 | Cohen syndrome | Microcephaly | |
| VPS13C | 15 | q22.2 | Parkinson disease autosomal recessive | Parkinsonism |
| VPS33B | 15 | q26.1 | Arthrogryposis renal dysfunction and cholestasis syndrome 2 (ARCS2) | Arthrogryposis spectrum | |
| VPS35 | 16 | q11.2 | Parkinson disease type 17 | Parkinsonism | |
| VRJS | 8 | q24.3 | VERHEIJ SYNDROME | Autism spectrum | |
| VRK1 | 14 | q32 | Pontocerebellar hypoplasia | Microcephaly | |
| VSX2 | 14 | q24.3 | Microphthalmia isolated with coloboma 3 (MCOPCB3) | Microphthalmia | |
| VWA3B | 2 | q11.2 | Spinocerebellar ataxia autosomal recessive type 22 | Ataxia spectrum | |