Variant Synonymizer: Platform to identify mutations defined in different ways is available now!

VarSy

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

Browse Summaries

Stats

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

Gene–Disease Browser

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Gene Disease Score Actions
CNBP
(HGNC:13164)
myotonic dystrophy
(MONDO_0016107)
Strong
CNBP
(HGNC:13164)
myotonic dystrophy type 2
(MONDO_0011266)
Strong
ZNF44
(HGNC:13110)
epilepsy
(MONDO_0005027)
Limited
ZNF41
(HGNC:13107)
intellectual disability
(MONDO_0001071)
Moderate
ZNF44
(HGNC:13110)
intellectual disability
(MONDO_0001071)
Limited
ZMYM5
(HGNC:13029)
intellectual disability
(MONDO_0001071)
Limited
ZNF202
(HGNC:12994)
myocardial ischemia
(MONDO_0024644)
Strong
ZNF224
(HGNC:13017)
Alzheimer disease
(MONDO_0004975)
Moderate
ZNF184
(HGNC:12975)
Parkinson disease
(MONDO_0005180)
Limited
ZNF182
(HGNC:13001)
intellectual disability
(MONDO_0001071)
Limited
SF1
(HGNC:12950)
multiple endocrine neoplasia type 1
(MONDO_0007540)
Disputed
ZBTB17
(HGNC:12936)
dilated cardiomyopathy
(MONDO_0005021)
Strong
TRIM26
(HGNC:12962)
schizophrenia
(MONDO_0005090)
Limited
ZNF142
(HGNC:12927)
neurodevelopmental disorder with impaired speech and hyperkinetic movements
(MONDO_0032741)
Strong
ZBTB16
(HGNC:12930)
acute promyelocytic leukemia
(MONDO_0012883)
Strong
XRN2
(HGNC:12836)
autism spectrum disorder
(MONDO_0005258)
Strong
ZNF141
(HGNC:12926)
Huntington disease
(MONDO_0007739)
Moderate
YME1L1
(HGNC:12843)
autism spectrum disorder
(MONDO_0005258)
Limited
ZNF12
(HGNC:12902)
autism
(MONDO_0005260)
Limited
YWHAH
(HGNC:12853)
schizophrenia
(MONDO_0005090)
Limited
Showing 6501–6520 of 6681