rs61753238(C;C)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs61753238 |
Gene | PEX7 |
Chromosome | 6 |
Position | 136,822,785 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
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 |