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rs8556

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs8556(C;T)
Make rs8556(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position48728228
GeneHOXB13
is asnp
is mentioned by
dbSNPrs8556
ebirs8556
HLIrs8556
Exacrs8556
Varsomers8556
Maprs8556
PheGenIrs8556
hapmaprs8556
1000 genomesrs8556
hgdprs8556
ensemblrs8556
gopubmedrs8556
geneviewrs8556
scholarrs8556
googlers8556
pharmgkbrs8556
gwascentralrs8556
openSNPrs8556
23andMers8556
23andMe allrs8556
SNP Nexus

SNPshotrs8556
SNPdbers8556
MSV3drs8556
GWAS Ctlgrs8556
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 25874003OA-icon.png] Synonymous Polymorphisms in HOXB13 as a Protective Factor for Prostate Cancer


ClinVar
Risk rs8556(A,T;A,T)
Alt rs8556(A,T;A,T)
Reference rs8556(C;C)
Significance Unknown
Disease not specified
Variation info
Gene HOXB13
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.46805590G>T
CLNSRC
CLNACC RCV000115970.3,