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rs753376100

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753376100(C;T)
Make rs753376100(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position3910664
GenePANK2
is asnp
is mentioned by
dbSNPrs753376100
dbSNP (classic)rs753376100
ClinGenrs753376100
ebirs753376100
HLIrs753376100
Exacrs753376100
Gnomadrs753376100
Varsomers753376100
LitVarrs753376100
Maprs753376100
PheGenIrs753376100
Biobankrs753376100
1000 genomesrs753376100
hgdprs753376100
ensemblrs753376100
geneviewrs753376100
scholarrs753376100
googlers753376100
pharmgkbrs753376100
gwascentralrs753376100
openSNPrs753376100
23andMers753376100
23andMe allrs753376100
SNPshotrs753376100
SNPdbers753376100
MSV3drs753376100
GWAS Ctlgrs753376100
Max Magnitude0
ClinVar
Risk rs753376100(T;T)
Alt rs753376100(T;T)
Reference Rs753376100(C;C)
Significance Pathogenic
Disease Neurodegeneration
Variation info
Gene PANK2
CLNDBN Neurodegeneration
Reversed 0
HGVS NC_000020.10:g.3891311C>T
CLNSRC
CLNACC RCV000414787.1,