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rs886041667(CG;CG)

From SNPedia
common in clinvar
Is agenotype
ofrs886041667
GeneHSPG2
Chromosome1
Position21,880,518
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 7.8 Schwartz Jampel syndrome type 1
(CG;CG) 0 common in clinvar

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