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rs863223303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223303(-;GA)
Make rs863223303(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position64767745
GeneSPTB
is asnp
is mentioned by
dbSNPrs863223303
ClinGenrs863223303
ebirs863223303
HLIrs863223303
Exacrs863223303
Varsomers863223303
Maprs863223303
PheGenIrs863223303
hapmaprs863223303
1000 genomesrs863223303
hgdprs863223303
ensemblrs863223303
gopubmedrs863223303
geneviewrs863223303
scholarrs863223303
googlers863223303
pharmgkbrs863223303
gwascentralrs863223303
openSNPrs863223303
23andMers863223303
23andMe allrs863223303
SNP Nexus

SNPshotrs863223303
SNPdbers863223303
MSV3drs863223303
GWAS Ctlgrs863223303
Max Magnitude0
ClinVar
Risk rs863223303(GA;GA)
Alt rs863223303(GA;GA)
Reference Rs863223303(-;-)
Significance Pathogenic
Disease Elliptocytosis 3
Variation info
Gene SPTB
CLNDBN Elliptocytosis 3
Reversed 1
HGVS NC_000014.8:g.65234464_65234465dupTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000013682.18,