RS63751229 PSEN1

Health Risk Chr 14:73198060
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What This Variant Does
"rs63751229, also known as P267S or Pro267Ser, is a SNP in the presenilin 1 PSEN1 gene. The rare rs63...
Associated Conditions
Alzheimer disease 3
Alzheimer disease 3
Frontotemporal dementia
Pick disease
Acne inversa
familial
3
Alzheimer disease 3
Acne inversa
familial
3
Frontotemporal dementia
Pick disease
Alzheimer disease 3
Alzheimer disease 3
Other Variants in PSEN1
rs63750306 rs63750590 rs63750526 rs63751235 rs661 rs63751037 rs63749885 rs63750231 rs63751272 rs63751223
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