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rs2141698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2141698(A;A)
Make rs2141698(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position172425667
GeneITGA6
is asnp
is mentioned by
dbSNPrs2141698
ebirs2141698
HLIrs2141698
Exacrs2141698
Varsomers2141698
Maprs2141698
PheGenIrs2141698
hapmaprs2141698
1000 genomesrs2141698
hgdprs2141698
ensemblrs2141698
gopubmedrs2141698
geneviewrs2141698
scholarrs2141698
googlers2141698
pharmgkbrs2141698
gwascentralrs2141698
openSNPrs2141698
23andMers2141698
23andMe allrs2141698
SNP Nexus

SNPshotrs2141698
SNPdbers2141698
MSV3drs2141698
GWAS Ctlgrs2141698
GMAF0.1465
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22148122OA-icon.png] A missense polymorphism (rs11895564, Ala380Thr) of integrin alpha 6 is associated with the development and progression of papillary thyroid carcinoma in Korean population