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Items: 3

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:198362018
GRCh38:
Chr2:197497294
HSPD1not specified, Spastic Paraplegia, DominantBenign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
2.
GRCh37:
Chr2:198363504
GRCh38:
Chr2:197498780
HSPD1not specified, Spastic Paraplegia, DominantBenign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
3.
GRCh37:
Chr2:198363546
GRCh38:
Chr2:197498822
HSPD1not specified, not provided, Spastic paraplegia,
Spastic Paraplegia, Dominant
Conflicting interpretations of pathogenicity
(Nov 26, 2016)
criteria provided, conflicting interpretations
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