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Items: 3

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr1:55523127
GRCh38:
Chr1:55057454
PCSK9Hypercholesterolemia, autosomal dominant, 3Pathogenic
(Feb 12, 2008)
no assertion criteria provided
2.
GRCh37:
Chr1:55518073
GRCh38:
Chr1:55052400
PCSK9Hypercholesterolemia, autosomal dominant, 3Pathogenic
(Feb 12, 2008)
no assertion criteria provided
3.
GRCh37:
Chr1:55509689
GRCh38:
Chr1:55044016
PCSK9Hypercholesterolemia, autosomal dominant, 3Pathogenic
(Feb 12, 2008)
no assertion criteria provided
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