RS794729671 GRN

Health Risk Chr 17:44352080
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What This Variant Does
"rs794729671, also known as c.1246dupT and p.Cys416Leufs, represents a very rare mutation in the GRN ...
Associated Conditions
Frontotemporal dementia
Cognitive impairment
Frontotemporal dementia
Cognitive impairment
Other Variants in GRN
rs63750077 rs63751006 rs63750331 rs606231220 rs63749801 rs606231221 rs63751243 rs63751294 rs63749877 rs2143337085
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