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rs267607086

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607086(C;T)
Make rs267607086(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position64772867
GeneSPTB
is asnp
is mentioned by
dbSNPrs267607086
ebirs267607086
HLIrs267607086
Exacrs267607086
Varsomers267607086
Maprs267607086
PheGenIrs267607086
hapmaprs267607086
1000 genomesrs267607086
hgdprs267607086
ensemblrs267607086
gopubmedrs267607086
geneviewrs267607086
scholarrs267607086
googlers267607086
pharmgkbrs267607086
gwascentralrs267607086
openSNPrs267607086
23andMers267607086
23andMe allrs267607086
SNP Nexus

SNPshotrs267607086
SNPdbers267607086
MSV3drs267607086
GWAS Ctlgrs267607086
Max Magnitude0
ClinVar
Risk rs267607086(T;T)
Alt rs267607086(T;T)
Reference rs267607086(C;C)
Significance Pathogenic
Disease Spherocytosis type 2
Variation info
Gene SPTB
CLNDBN Spherocytosis type 2
Reversed 1
HGVS NC_000014.8:g.65239585G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013696.17,