RS121908952 PAPSS2

Health Risk Chr 10:87727403
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What This Variant Does
"[OMIM:?]
Associated Conditions
Spondyloepimetaphyseal dysplasia
PAPSS2 type
Autosomal recessive brachyolmia
Spondyloepimetaphyseal dysplasia
PAPSS2 type
Autosomal recessive brachyolmia
Other Variants in PAPSS2
rs121908950 rs121908951 rs606231241 rs606231242 rs786200933 rs606231243 rs786200934 rs794727710 rs797045099 rs138943074
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