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rs748538823

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748538823(C;T)
Make rs748538823(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position232819834
GeneGIGYF2
is asnp
is mentioned by
dbSNPrs748538823
ebirs748538823
HLIrs748538823
Exacrs748538823
Varsomers748538823
Maprs748538823
PheGenIrs748538823
hapmaprs748538823
1000 genomesrs748538823
hgdprs748538823
ensemblrs748538823
gopubmedrs748538823
geneviewrs748538823
scholarrs748538823
googlers748538823
pharmgkbrs748538823
gwascentralrs748538823
openSNPrs748538823
23andMers748538823
23andMe allrs748538823
SNP Nexus

SNPshotrs748538823
SNPdbers748538823
MSV3drs748538823
GWAS Ctlgrs748538823
Max Magnitude0
ClinVar
Risk rs748538823(T;T)
Alt rs748538823(T;T)
Reference rs748538823(C;C)
Significance Probable-Pathogenic
Disease Parkinson disease 11
Variation info
Gene GIGYF2
CLNDBN Parkinson disease 11
Reversed 0
HGVS NC_000002.11:g.233684544C>T
CLNSRC
CLNACC RCV000198246.1,