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rs116074753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs116074753(A;C)
Make rs116074753(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position232794835
GeneGIGYF2
is asnp
is mentioned by
dbSNPrs116074753
ebirs116074753
HLIrs116074753
Exacrs116074753
Varsomers116074753
Maprs116074753
PheGenIrs116074753
hapmaprs116074753
1000 genomesrs116074753
hgdprs116074753
ensemblrs116074753
gopubmedrs116074753
geneviewrs116074753
scholarrs116074753
googlers116074753
pharmgkbrs116074753
gwascentralrs116074753
openSNPrs116074753
23andMers116074753
23andMe allrs116074753
SNP Nexus

SNPshotrs116074753
SNPdbers116074753
MSV3drs116074753
GWAS Ctlgrs116074753
GMAF0.0004591
Max Magnitude0
OMIM612003
Desc
Variant0002
Relatedalso
ClinVar
Risk rs116074753(C,G;C,G)
Alt rs116074753(C,G;C,G)
Reference rs116074753(A;A)
Significance Other
Disease Parkinson disease 11
Variation info
Gene GIGYF2
CLNDBN Parkinson disease 11
Reversed 0
HGVS NC_000002.11:g.233659545A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000790.4,