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rs61753238(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs61753238
GenePEX7
Chromosome6
Position136,822,785
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 carrier of one Rhizomelic Chondrodysplasia Punctata Type I disorder allele
(G;G) 7 Rhizomelic Chondrodysplasia Punctata Type I disorder