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rs515726214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726214(A;T)
Make rs515726214(T;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position43216262
GeneEPB42
is asnp
is mentioned by
dbSNPrs515726214
ebirs515726214
HLIrs515726214
Exacrs515726214
Varsomers515726214
Maprs515726214
PheGenIrs515726214
hapmaprs515726214
1000 genomesrs515726214
hgdprs515726214
ensemblrs515726214
gopubmedrs515726214
geneviewrs515726214
scholarrs515726214
googlers515726214
pharmgkbrs515726214
gwascentralrs515726214
openSNPrs515726214
23andMers515726214
23andMe allrs515726214
SNP Nexus

SNPshotrs515726214
SNPdbers515726214
MSV3drs515726214
GWAS Ctlgrs515726214
Max Magnitude0
ClinVar
Risk rs515726214(T;T)
Alt rs515726214(T;T)
Reference rs515726214(A;A)
Significance Pathogenic
Disease Spherocytosis type 5
Variation info
Gene EPB42
CLNDBN Spherocytosis type 5
Reversed 0
HGVS NC_000015.9:g.43508460A>T
CLNSRC ClinVar
CLNACC RCV000119055.2,