RS137853100 PROP1

Health Risk Chr 5:177994151 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pituitary hormone deficiency
combined
2
Inborn genetic diseases
Combined pituitary hormone deficiencies
genetic form
Pituitary hormone deficiency
combined
2
Inborn genetic diseases
Combined pituitary hormone deficiencies
genetic form
Population Frequencies
gnomAD ALL
0%
Other Variants in PROP1
rs121917839 rs121917840 rs587776681 rs193922688 rs121917841 rs587776682 rs587776683 rs121917842 rs121917843 rs121917844
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