RS797044908 PHF6

Health Risk Chr X:134417249
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in PHF6
rs132630297 rs132630298 rs104894917 rs132630299 rs104894918 rs132630300 rs104894919 rs132630301 rs771399346 rs758791658
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