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rs515726212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726212(A;A)
Make rs515726212(A;G)
ReferenceGRCh38 38.1/142
Chromosome15
Position43208749
GeneEPB42
is asnp
is mentioned by
dbSNPrs515726212
ebirs515726212
HLIrs515726212
Exacrs515726212
Varsomers515726212
Maprs515726212
PheGenIrs515726212
hapmaprs515726212
1000 genomesrs515726212
hgdprs515726212
ensemblrs515726212
gopubmedrs515726212
geneviewrs515726212
scholarrs515726212
googlers515726212
pharmgkbrs515726212
gwascentralrs515726212
openSNPrs515726212
23andMers515726212
23andMe allrs515726212
SNP Nexus

SNPshotrs515726212
SNPdbers515726212
MSV3drs515726212
GWAS Ctlgrs515726212
Max Magnitude0
ClinVar
Risk rs515726212(A;A)
Alt rs515726212(A;A)
Reference rs515726212(G;G)
Significance Pathogenic
Disease Spherocytosis type 5
Variation info
Gene EPB42
CLNDBN Spherocytosis type 5
Reversed 0
HGVS NC_000015.9:g.43500947G>A
CLNSRC ClinVar
CLNACC RCV000119052.2,