VASH2, vasohibin 2, 79805

N. diseases: 45; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3002288
rs3002288
Entrez Id: 79805
Gene Symbol: VASH2
VASH2
CUI: C0015396
Disease:
Eye Color
A 0.800 GeneticVariation GWASCAT Using blue, intermediate (including green) and brown eye colors as co-dominant outcomes, we identified the SNP rs3002288 in VASH2 on 1q32.3 associated with brown eye (P = 7.0 × 10(-8); P = 5.3 × 10(-5) in the discovery set and P = 0.02 in the replication set). 23548203 2013
dbSNP: rs3002288
rs3002288
Entrez Id: 79805
Gene Symbol: VASH2
VASH2
CUI: C0015396
Disease:
Eye Color
A 0.800 GeneticVariation GWASDB Using blue, intermediate (including green) and brown eye colors as co-dominant outcomes, we identified the SNP rs3002288 in VASH2 on 1q32.3 associated with brown eye (P = 7.0 × 10(-8); P = 5.3 × 10(-5) in the discovery set and P = 0.02 in the replication set). 23548203 2013
dbSNP: rs374073809
rs374073809
Entrez Id: 79805
Gene Symbol: VASH2
VASH2
CUI: C3714756
Disease:
Intellectual Disability
0.010 GeneticVariation BEFREE We identified a founder, homozygous stop-gain variant in SVBP (c.82C>T; p.[Gln28*]) in four affected individuals from two independent families with intellectual disability, microcephaly, ataxia, and muscular hypotonia. 30607023 2019