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rs28929478

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
(G;G) 0 common in clinvar
Make rs28929478(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position110281857
GeneATP2A2
is asnp
is mentioned by
dbSNPrs28929478
dbSNP (classic)rs28929478
ClinGenrs28929478
ebirs28929478
HLIrs28929478
Exacrs28929478
Gnomadrs28929478
Varsomers28929478
LitVarrs28929478
Maprs28929478
PheGenIrs28929478
Biobankrs28929478
1000 genomesrs28929478
hgdprs28929478
ensemblrs28929478
geneviewrs28929478
scholarrs28929478
googlers28929478
pharmgkbrs28929478
gwascentralrs28929478
openSNPrs28929478
23andMers28929478
SNPshotrs28929478
SNPdbers28929478
MSV3drs28929478
GWAS Ctlgrs28929478
Max Magnitude0
OMIM108740
DescDARIER DISEASE
Variant0001
Relatedalso


ClinVar
Risk Rs28929478(A;A)
Alt Rs28929478(A;A)
Reference Rs28929478(G;G)
Significance Pathogenic
Disease Keratosis follicularis not provided
Variation info
Gene ATP2A2
CLNDBN Keratosis follicularis not provided
Reversed 0
HGVS NC_000012.11:g.110719662G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000019367.28, RCV000414388.1,