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rs1253871

From SNPedia

Merged intors819760
Orientationplus
Stabilizedplus
Make rs1253871(C;C)
Make rs1253871(C;T)
Make rs1253871(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position99244586
is asnp
is mentioned by
dbSNPrs1253871
ebirs1253871
HLIrs1253871
Exacrs1253871
Varsomers1253871
Maprs1253871
PheGenIrs1253871
hapmaprs1253871
1000 genomesrs1253871
hgdprs1253871
ensemblrs1253871
gopubmedrs1253871
geneviewrs1253871
scholarrs1253871
googlers1253871
pharmgkbrs1253871
gwascentralrs1253871
openSNPrs1253871
23andMers1253871
23andMe allrs1253871
SNP Nexus

SNPshotrs1253871
SNPdbers1253871
MSV3drs1253871
GWAS Ctlgrs1253871
StatusMerged into rs819760
Max Magnitude

[PMID 25511740] Identification of epidermal growth factor receptor (EGFR) genetic variants that modify risk for head and neck squamous cell carcinoma