Cone-rod Dystrophy
Other
188 variants
23 genes
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Associated Genes (23)
ABCA4
PRPH2
USH2A
TTLL5
ERCC6
CABP4
NR2E3
EYS
RHO
RDH12
CERKL
CNGB3
AIPL1
CRB1
ADAM9
CRX
GUCY2D
FAM161A
CNGA1
SGSH
NMNAT1
MYO7A
CDH23
Associated Variants (188)
RSID
Gene
Risk Allele
Odds Ratio
Evidence
RS61750155
ABCA4
—
—
strong
RS61755775
PRPH2
—
—
strong
RS61754402
PRPH2
—
—
strong
RS61755781
PRPH2
—
—
strong
RS61755813
PRPH2
—
—
strong
RS281865373
PRPH2
—
—
strong
RS61748434
PRPH2
—
—
strong
RS61754030
ABCA4
—
—
strong
RS61750065
ABCA4
—
—
strong
RS62645946
ABCA4
—
—
strong
RS61750146
ABCA4
—
—
strong
RS281865377
ABCA4
—
—
strong
RS1762111
ABCA4
—
—
strong
RS61752435
ABCA4
—
—
strong
RS62646872
ABCA4
—
—
strong
RS61751407
ABCA4
—
—
strong
RS61751418
ABCA4
—
—
strong
RS483353055
USH2A
—
—
strong
RS587777469
TTLL5
—
—
strong
RS139007661
ERCC6
—
—
strong
RS61760163
ERCC6
—
—
strong
RS150115958
CABP4
—
—
strong
RS2723341
NR2E3
—
—
strong
RS201652272
EYS
—
—
strong
RS2523765410
ABCA4
—
—
strong
RS104893793
RHO
—
—
strong
RS28940314
RDH12
—
—
strong
RS121434337
RDH12
—
—
strong
RS80338903
USH2A
—
—
strong
RS121909398
CERKL
—
—
strong
RS397515360
CNGB3
—
—
strong
RS281865195
AIPL1
—
—
strong
RS62635654
CRB1
—
—
strong
RS137853041
ADAM9
—
—
strong
RS786205086
ADAM9
—
—
strong
RS104894672
CRX
—
—
strong
RS61748436
CRX
—
—
strong
RS61750173
GUCY2D
—
—
strong
RS200691042
FAM161A
—
—
strong
RS61755792
PRPH2
—
—
strong
RS61755786
PRPH2
—
—
strong
RS121918567
PRPH2
—
—
strong
RS62625014
CNGA1
—
—
strong
RS138504221
SGSH
—
—
strong
RS150726175
NMNAT1
—
—
strong
RS200641606
MYO7A
—
—
strong
RS115113440
CDH23
—
—
strong
RS397517974
USH2A
—
—
strong
RS397517994
USH2A
—
—
strong
RS142326926
AIPL1
—
—
strong
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