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rs118203903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118203903(C;G)
Make rs118203903(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position232809731
GeneGIGYF2
is asnp
is mentioned by
dbSNPrs118203903
ebirs118203903
HLIrs118203903
Exacrs118203903
Varsomers118203903
Maprs118203903
PheGenIrs118203903
hapmaprs118203903
1000 genomesrs118203903
hgdprs118203903
ensemblrs118203903
gopubmedrs118203903
geneviewrs118203903
scholarrs118203903
googlers118203903
pharmgkbrs118203903
gwascentralrs118203903
openSNPrs118203903
23andMers118203903
23andMe allrs118203903
SNP Nexus

SNPshotrs118203903
SNPdbers118203903
MSV3drs118203903
GWAS Ctlgrs118203903
Max Magnitude0
OMIM612003
Desc
Variant0003
Relatedalso
ClinVar
Risk rs118203903(G;G)
Alt rs118203903(G;G)
Reference rs118203903(C;C)
Significance Other
Disease Parkinson disease 11
Variation info
Gene GIGYF2
CLNDBN Parkinson disease 11
Reversed 0
HGVS NC_000002.11:g.233674441C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000791.4,