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rs767649

From SNPedia

Orientationplus
Make rs767649(A;A)
Make rs767649(A;T)
Make rs767649(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position25572410
GeneLOC105372754, MIR155, MIR155HG
is asnp
is mentioned by
dbSNPrs767649
ebirs767649
HLIrs767649
Exacrs767649
Varsomers767649
Maprs767649
PheGenIrs767649
hapmaprs767649
1000 genomesrs767649
hgdprs767649
ensemblrs767649
gopubmedrs767649
geneviewrs767649
scholarrs767649
googlers767649
pharmgkbrs767649
gwascentralrs767649
openSNPrs767649
23andMers767649
23andMe allrs767649
SNP Nexus

SNPshotrs767649
SNPdbers767649
MSV3drs767649
GWAS Ctlgrs767649
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 26543233] A functional variant in miR-155 regulation region contributes to lung cancer risk and survival