RS121918237 SLC34A3

Health Risk Chr 9:137233234
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What This Variant Does
"rs121918237, also known as c.586G&gt
Associated Conditions
Autosomal recessive hypophosphatemic bone disease
Autosomal recessive hypophosphatemic bone disease
Other Variants in SLC34A3
rs794729658 rs121918234 rs121918235 rs121918236 rs794729659 rs121918238 rs1554784044 rs121918239 rs1554784508 rs199536442
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