RS77722678 FGFR3

Health Risk Chr 4:1805643
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What This Variant Does
"rs77722678, also known as c.1619A&gt
Associated Conditions
Hypochondroplasia
Hypochondroplasia
Inborn genetic diseases
Achondroplasia
Neurodevelopmental delay
Hypochondroplasia
Hypochondroplasia
Inborn genetic diseases
Achondroplasia
Neurodevelopmental delay
Other Variants in FGFR3
rs28931614 rs28931615 rs75790268 rs78311289 rs121913482 rs121913484 rs121913101 rs121913103 rs28933068 rs121913483
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