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rs201106962

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201106962(A;C)
Make rs201106962(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position89828156
GeneSNCA
is asnp
is mentioned by
dbSNPrs201106962
ebirs201106962
HLIrs201106962
Exacrs201106962
Varsomers201106962
Maprs201106962
PheGenIrs201106962
hapmaprs201106962
1000 genomesrs201106962
hgdprs201106962
ensemblrs201106962
gopubmedrs201106962
geneviewrs201106962
scholarrs201106962
googlers201106962
pharmgkbrs201106962
gwascentralrs201106962
openSNPrs201106962
23andMers201106962
23andMe allrs201106962
SNP Nexus

SNPshotrs201106962
SNPdbers201106962
MSV3drs201106962
GWAS Ctlgrs201106962
Max Magnitude0
ClinVar
Risk rs201106962(C;C)
Alt rs201106962(C;C)
Reference rs201106962(A;A)
Significance Pathogenic
Disease Parkinson disease 1
Variation info
Gene SNCA
CLNDBN Parkinson disease 1
Reversed 0
HGVS NC_000004.11:g.90749307A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000149507.3,