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rs2317676

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2317676(A;G)
Make rs2317676(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position47310917
GeneITGB3, THCAT158
is asnp
is mentioned by
dbSNPrs2317676
dbSNP (classic)rs2317676
ClinGenrs2317676
ebirs2317676
HLIrs2317676
Exacrs2317676
Gnomadrs2317676
Varsomers2317676
LitVarrs2317676
Maprs2317676
PheGenIrs2317676
Biobankrs2317676
1000 genomesrs2317676
hgdprs2317676
ensemblrs2317676
geneviewrs2317676
scholarrs2317676
googlers2317676
pharmgkbrs2317676
gwascentralrs2317676
openSNPrs2317676
23andMers2317676
SNPshotrs2317676
SNPdbers2317676
MSV3drs2317676
GWAS Ctlgrs2317676
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 24777809] SNPs in MicroRNA-Binding Sites in the ITGB1 and ITGB3 3'-UTR Increase Colorectal Cancer Risk


ClinVar
Risk rs2317676(G;G)
Alt rs2317676(G;G)
Reference Rs2317676(A;A)
Significance Probable-non-pathogenic
Disease Glanzmann thrombasthenia
Variation info
Gene ITGB3 THCAT158
CLNDBN Glanzmann thrombasthenia
Reversed 0
HGVS NC_000017.10:g.45388283A>G
CLNSRC
CLNACC RCV000310133.1,