RS104894361 KRAS

Health Risk Chr 12:25245369 snv missense variant
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What This Variant Does
"aka c.15A&gt
Associated Conditions
Cardiofaciocutaneous syndrome 2
Inborn genetic diseases
RASopathy
Cardiofaciocutaneous syndrome 2
Inborn genetic diseases
RASopathy
Population Frequencies
gnomAD ALL
100%
Other Variants in KRAS
rs121913530 rs112445441 rs121913528 rs121913529 rs606231202 rs104894359 rs104894360 rs104894364 rs104894365 rs104894366
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