SNP information rs34778348
Normal allele: GG
LRRK2 variant is a risk factor for sporadic Parkinson's disease
Polymorphism rs34778348 is related to topics like this:
A disorder that progresses gradually within the nervous system is known as Parkinson's disease. It...
Research and publications:
16172858 Pathogenic Lrrk2 substitutions in Parkinson's disease.
17659642 Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians.
18688798 Lrrk2 R1628P in non-Chinese Asian races.
18704525 Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.
19343804 LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
19854095 The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population.
20186690 Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.
20301387 LRRK2 Parkinson Disease.
21885347 Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.
22373437 Identification of functional genetic variation in exome sequence analysis.
23651603 P268S in NOD2 is associated with Parkinson's disease susceptibility in a Chinese population.
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