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#601800 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3; SHEP3
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8, INCLUDED
Cytogenetic locations: 17952075
Gene summaries Genetic tests Medical literature
#611724 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 8; SHEP8
#227220 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1; SHEP1
Cytogenetic locations: 1p36, 1p36
#266300 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2; SHEP2
UV-INDUCED SKIN DAMAGE, SUSCEPTIBILITY TO, INCLUDED
Cytogenetic locations: Fish-eye
#227240 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5; SHEP5
Cytogenetic locations: 5p15.33
#210750 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6; SHEP6
#612267 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 10; SHEP10
Cytogenetic locations: -
#611742 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 9; SHEP9
Cytogenetic locations: 617888
%300843 - BORNHOLM EYE DISEASE; BED
Cytogenetic locations: 15197065
#113750 - ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 4, INCLUDED; SHEP4, INCLUDED
Cytogenetic locations: 23364476
#612271 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11; SHEP11
Cytogenetic locations: 18488028
#300600 - ALAND ISLAND EYE DISEASE; AIED
Cytogenetic locations: 1st
%180020 - RETINAL CONE DYSTROPHY 1; RCD1
Cytogenetic locations: 11583655
#612657 - CONE-ROD DYSTROPHY 12; CORD12
Cytogenetic locations: 18654668
#616170 - MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD
Cytogenetic locations: 25227500
#180105 - RETINITIS PIGMENTOSA 10; RP10
Cytogenetic locations: 17635473
#617460 - RETINITIS PIGMENTOSA 79; RP79
Cytogenetic locations: 602809
#614932 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13
Cytogenetic locations: 23084291
#613660 - CONE-ROD DYSTROPHY 15; CORD15
RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED
Cytogenetic locations: 28765526
#613862 - RETINITIS PIGMENTOSA 38; RP38
Cytogenetic locations: 600531
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