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rs551660089

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs551660089(A;A)
Make rs551660089(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position28894244
GeneATP2A1
is asnp
is mentioned by
dbSNPrs551660089
dbSNP (classic)rs551660089
ClinGenrs551660089
ebirs551660089
HLIrs551660089
Exacrs551660089
Gnomadrs551660089
Varsomers551660089
LitVarrs551660089
Maprs551660089
PheGenIrs551660089
Biobankrs551660089
1000 genomesrs551660089
hgdprs551660089
ensemblrs551660089
geneviewrs551660089
scholarrs551660089
googlers551660089
pharmgkbrs551660089
gwascentralrs551660089
openSNPrs551660089
23andMers551660089
23andMe allrs551660089
SNPshotrs551660089
SNPdbers551660089
MSV3drs551660089
GWAS Ctlgrs551660089
Max Magnitude0
ClinVar
Risk rs551660089(A;A)
Alt rs551660089(A;A)
Reference Rs551660089(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NPIPB8 ATP2A1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.28905565G>A
CLNSRC
CLNACC RCV000424927.1,