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rs115735611

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs115735611(A;G)
Make rs115735611(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position232791426
GeneGIGYF2
is asnp
is mentioned by
dbSNPrs115735611
ebirs115735611
HLIrs115735611
Exacrs115735611
Varsomers115735611
Maprs115735611
PheGenIrs115735611
hapmaprs115735611
1000 genomesrs115735611
hgdprs115735611
ensemblrs115735611
gopubmedrs115735611
geneviewrs115735611
scholarrs115735611
googlers115735611
pharmgkbrs115735611
gwascentralrs115735611
openSNPrs115735611
23andMers115735611
23andMe allrs115735611
SNP Nexus

SNPshotrs115735611
SNPdbers115735611
MSV3drs115735611
GWAS Ctlgrs115735611
Max Magnitude0
ClinVar
Risk rs115735611(G;G)
Alt rs115735611(G;G)
Reference rs115735611(A;A)
Significance Other
Disease Parkinson disease 11
Variation info
Gene GIGYF2
CLNDBN Parkinson disease 11
Reversed 0
HGVS NC_000002.11:g.233656136A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000793.4,