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rs745452577(G;G)
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common in clinvar
Is a
genotype
of
rs745452577
Gene
HSPG2
Chromosome
1
Position
21,865,798
mentioned
by
Magnitude
0
Repute
Good
Geno
Mag
Summary
(A;G)
1
Of uncertain significance relative to Schwartz Jampel syndrome according to ClinVar
(G;G)
0
common in clinvar
Category
:
Is a genotype
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