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*616153 - SOLUTE CARRIER FAMILY 25, MEMBER 52; SLC25A52
Cytogenetic locations: 23266187
Gene summaries Genetic tests Medical literature
%610209 - MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11
Cytogenetic locations: 11836652
*604017 - UDP-GAL:BETA-GlcNAc BETA-1,4-GALACTOSYLTRANSFERASE, POLYPEPTIDE 6; B4GALT6
Cytogenetic locations: 17q25.3
*614136 - TRAFFICKING PROTEIN PARTICLE COMPLEX, SUBUNIT 8; TRAPPC8
Cytogenetic locations: ########
*603577 - NUCLEOLAR PROTEIN 4; NOL4
Cytogenetic locations: 12644935
*600389 - MEPRIN, BETA SUBUNIT; MEP1B
Cytogenetic locations: 12556482
#619226 - BLISTERING, ACANTHOLYTIC, OF ORAL AND LARYNGEAL MUCOSA; ABOLM
*125643 - DESMOCOLLIN 1; DSC1
Cytogenetic locations: #7679953
#145680 - HYPERTHYROXINEMIA, DYSTRANSTHYRETINEMIC; DTTRH
Cytogenetic locations: 03935040
*616319 - RING FINGER PROTEIN 138; RNF138
Cytogenetic locations: 618461
*613772 - KELCH-LIKE 14; KLHL14
Cytogenetic locations: 10718198
*617998 - GRB2-ASSOCIATED REGULATOR OF MAPK1, SUBTYPE 1; GAREM1
Cytogenetic locations: 19509291
#612877 - CARDIOMYOPATHY, DILATED, 1BB; CMD1BB
Cytogenetic locations: 33949662
#619957 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER 8; ADHD8
Cytogenetic locations: 602770
#610193 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10
Cytogenetic locations: 17105751
#616260 - TENORIO SYNDROME; TNORS
#615508 - ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE
Cytogenetic locations: 23974871
#620971 - MYOPATHY WITH MYALGIA, INCREASED SERUM CREATINE KINASE, AND WITH OR WITHOUT EPISODIC RHABDOMYOLYSIS 2; MMCKR2
#616734 - SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2
*600271 - DESMOCOLLIN 3; DSC3
Cytogenetic locations: 608546
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