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rs1194338

From SNPedia

Orientationplus
Stabilizedplus
Make rs1194338(A;A)
Make rs1194338(A;C)
Make rs1194338(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position65493967
is asnp
is mentioned by
dbSNPrs1194338
dbSNP (old)rs1194338
ClinGenrs1194338
ebirs1194338
HLIrs1194338
Exacrs1194338
Gnomadrs1194338
Varsomers1194338
LitVarrs1194338
Maprs1194338
PheGenIrs1194338
Biobankrs1194338
1000 genomesrs1194338
hgdprs1194338
ensemblrs1194338
gopubmedrs1194338
geneviewrs1194338
scholarrs1194338
googlers1194338
pharmgkbrs1194338
gwascentralrs1194338
openSNPrs1194338
23andMers1194338
23andMe allrs1194338
SNPshotrs1194338
SNPdbers1194338
MSV3drs1194338
GWAS Ctlgrs1194338
Max Magnitude

[PMID 29190941OA-icon.png] Associations between novel genetic variants in the promoter region of MALAT1 and risk of colorectal cancer.