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Over 2,000 gene–disease validation summaries are now available—no login required!

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Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
KLRG2
(HGNC:24778)
prostate cancer
(MONDO_0008315)
 Limited
PTCD3
(HGNC:24717)
Leigh syndrome
(MONDO_0009723)
 Strong
CIBAR2
(HGNC:24781)
Crohn disease
(MONDO_0005011)
 Disputed
FBLP1
(HGNC:24686)
chronic recurrent multifocal osteomyelitis
(MONDO_0009813)
 Limited
DCBLD2
(HGNC:24627)
relapsing polychondritis
(MONDO_0019125)
 Limited
VWA2
(HGNC:24709)
chronic kidney disease
(MONDO_0005300)
 Limited
GPATCH1
(HGNC:24658)
osteoporosis
(MONDO_0005298)
 Limited
FIGLA
(HGNC:24669)
premature menopause
(MONDO_0001119)
 Moderate
DNAJC10
(HGNC:24637)
Parkinson disease
(MONDO_0005180)
 Limited
CXXC4
(HGNC:24593)
myelodysplastic syndrome
(MONDO_0018881)
 Limited
CSNK2A2
(HGNC:2459)
type 2 diabetes mellitus
(MONDO_0005148)
 Limited
RPAP1
(HGNC:24567)
breast cancer
(MONDO_0007254)
 Limited
GINS2
(HGNC:24575)
Meier-Gorlin syndrome
(MONDO_0016817)
 Limited
DCAF13
(HGNC:24535)
neuromuscular disease
(MONDO_0019056)
 Limited
TMEM98
(HGNC:24529)
nanophthalmia
(MONDO_0005514)
 Strong
MPC2
(HGNC:24515)
schizophrenia
(MONDO_0005090)
 Limited
MPC2
(HGNC:24515)
bipolar disorder
(MONDO_0004985)
 Limited
NEPRO
(HGNC:24496)
anauxetic dysplasia 1
(MONDO_0054560)
 Limited
NEPRO
(HGNC:24496)
anauxetic dysplasia
(MONDO_0011773)
 Moderate
NEPRO
(HGNC:24496)
cartilage-hair hypoplasia
(MONDO_0009595)
 Limited
Showing 5881–5900 of 6681