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rs768091663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768091663(C;C)
Make rs768091663(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position20637956
GenePINK1
is asnp
is mentioned by
dbSNPrs768091663
dbSNP (classic)rs768091663
ClinGenrs768091663
ebirs768091663
HLIrs768091663
Exacrs768091663
Gnomadrs768091663
Varsomers768091663
LitVarrs768091663
Maprs768091663
PheGenIrs768091663
Biobankrs768091663
1000 genomesrs768091663
hgdprs768091663
ensemblrs768091663
geneviewrs768091663
scholarrs768091663
googlers768091663
pharmgkbrs768091663
gwascentralrs768091663
openSNPrs768091663
23andMers768091663
23andMe allrs768091663
SNPshotrs768091663
SNPdbers768091663
MSV3drs768091663
GWAS Ctlgrs768091663
Max Magnitude0
ClinVar
Risk rs768091663(C;C)
Alt rs768091663(C;C)
Reference Rs768091663(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PINK1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.20964449G>C
CLNSRC
CLNACC RCV000494163.1,