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#620410 - LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3; LDLCQ3
STATINS, RESPONSE TO, INCLUDED
Cytogenetic locations: 5q13.2
Gene summaries Genetic tests Medical literature
#620375 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 28; LGMDR28
#619864 - LEUKODYSTROPHY, CHILDHOOD-ONSET, REMITTING; CORLK
#619538 - CEREBRAL CAVERNOUS MALFORMATIONS 4; CCM4
#619324 - HYPERTRIGLYCERIDEMIA 2; HYTG2
Cytogenetic locations: ###a##
#619281 - IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE; IMD14B
Cytogenetic locations: 1p36.22
#619086 - DEAFNESS, AUTOSOMAL DOMINANT 79; DFNA79
Cytogenetic locations: PD#F##
#619030 - SKELETAL MUSCLE GLYCOGEN CONTENT AND METABOLISM QUANTITATIVE TRAIT LOCUS; SMGMQTL
Cytogenetic locations: #y####
#619016 - IFAP SYNDROME 2; IFAP2
Cytogenetic locations: PER1
#618858 - DIABETES MELLITUS, PERMANENT NEONATAL, 4; PNDM4
Cytogenetic locations: 11p15.5
#618420 - SPERMATOGENIC FAILURE 36; SPGF36
#618419 - MYOECTODERMAL GONADAL DYSGENESIS SYNDROME; MEGD
#618354 - HOUGE-JANSSENS SYNDROME 3; HJS3
Cytogenetic locations: 610499
*618262 - cAMP RESPONSE ELEMENT-BINDING PROTEIN 5; CREB5
Cytogenetic locations: #########c#
#617807 - NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW
#617137 - FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2
Cytogenetic locations: Snap91
#616638 - SMITH-KINGSMORE SYNDROME; SKS
#616362 - HOUGE-JANSSENS SYNDROME 2; HJS2
Cytogenetic locations: #$#(##
#616355 - HOUGE-JANSSENS SYNDROME 1; HJS1
#616282 - SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73
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