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rs864309650

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309650(C;T)
Make rs864309650(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position56104344
GeneCHCHD2
is asnp
is mentioned by
dbSNPrs864309650
ebirs864309650
HLIrs864309650
Exacrs864309650
Varsomers864309650
Maprs864309650
PheGenIrs864309650
hapmaprs864309650
1000 genomesrs864309650
hgdprs864309650
ensemblrs864309650
gopubmedrs864309650
geneviewrs864309650
scholarrs864309650
googlers864309650
pharmgkbrs864309650
gwascentralrs864309650
openSNPrs864309650
23andMers864309650
23andMe allrs864309650
SNP Nexus

SNPshotrs864309650
SNPdbers864309650
MSV3drs864309650
GWAS Ctlgrs864309650
Max Magnitude0
ClinVar
Risk rs864309650(T;T)
Alt rs864309650(T;T)
Reference rs864309650(C;C)
Significance Pathogenic
Disease Parkinson disease 22
Variation info
Gene CHCHD2
CLNDBN Parkinson disease 22, autosomal dominant
Reversed 1
HGVS NC_000007.13:g.56172037G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203229.1,