RS121918239 SLC34A3

Health Risk Chr 9:137233404
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What This Variant Does
"rs121918239, also known as c.756G&gt
Associated Conditions
Autosomal recessive hypophosphatemic bone disease
SLC34A3-related disorder
Thyroid cancer
nonmedullary
1
Clear cell carcinoma of kidney
Autosomal recessive hypophosphatemic bone disease
SLC34A3-related disorder
Thyroid cancer
nonmedullary
1
Clear cell carcinoma of kidney
Other Variants in SLC34A3
rs794729658 rs121918234 rs121918235 rs121918236 rs794729659 rs121918237 rs121918238 rs1554784044 rs1554784508 rs199536442
Ask Dr. Hemsworth about this variant