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rs231755

From SNPedia

Orientationminus
Stabilizedminus
Make rs231755(C;C)
Make rs231755(C;G)
Make rs231755(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position203888846
is asnp
is mentioned by
dbSNPrs231755
dbSNP (old)rs231755
ClinGenrs231755
ebirs231755
HLIrs231755
Exacrs231755
Gnomadrs231755
Varsomers231755
Maprs231755
PheGenIrs231755
Biobankrs231755
1000 genomesrs231755
hgdprs231755
ensemblrs231755
gopubmedrs231755
geneviewrs231755
scholarrs231755
googlers231755
pharmgkbrs231755
gwascentralrs231755
openSNPrs231755
23andMers231755
23andMe allrs231755
SNPshotrs231755
SNPdbers231755
MSV3drs231755
GWAS Ctlgrs231755
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 28052683] Cytotoxic T Lymphocyte-Associated Antigen 4 rs231775 polymorphism and Osteosarcoma: an updated systematic review and meta-analysis.