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rs17556

From SNPedia

Orientationminus
Stabilizedminus
Make rs17556(G;G)
Make rs17556(G;T)
Make rs17556(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101862596
is asnp
is mentioned by
dbSNPrs17556
ebirs17556
HLIrs17556
Exacrs17556
Varsomers17556
Maprs17556
PheGenIrs17556
hapmaprs17556
1000 genomesrs17556
hgdprs17556
ensemblrs17556
gopubmedrs17556
geneviewrs17556
scholarrs17556
googlers17556
pharmgkbrs17556
gwascentralrs17556
openSNPrs17556
23andMers17556
23andMe allrs17556
SNP Nexus

SNPshotrs17556
SNPdbers17556
MSV3drs17556
GWAS Ctlgrs17556
GMAF0.01088
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 22621753] Higher risk of matrix metalloproteinase (MMP-2, 7, 9) and tissue inhibitor of metalloproteinase (TIMP-2) genetic variants to gallbladder cancer