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rs762879569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762879569(A;A)
Make rs762879569(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position3907941
GenePANK2
is asnp
is mentioned by
dbSNPrs762879569
dbSNP (classic)rs762879569
ClinGenrs762879569
ebirs762879569
HLIrs762879569
Exacrs762879569
Gnomadrs762879569
Varsomers762879569
LitVarrs762879569
Maprs762879569
PheGenIrs762879569
Biobankrs762879569
1000 genomesrs762879569
hgdprs762879569
ensemblrs762879569
geneviewrs762879569
scholarrs762879569
googlers762879569
pharmgkbrs762879569
gwascentralrs762879569
openSNPrs762879569
23andMers762879569
23andMe allrs762879569
SNPshotrs762879569
SNPdbers762879569
MSV3drs762879569
GWAS Ctlgrs762879569
Max Magnitude0
ClinVar
Risk rs762879569(A;A)
Alt rs762879569(A;A)
Reference Rs762879569(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PANK2
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.3888588G>A
CLNSRC
CLNACC RCV000493982.1,