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rs1044243

From SNPedia

Orientationplus
Stabilizedplus
Make rs1044243(C;C)
Make rs1044243(C;T)
Make rs1044243(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position105541676
GeneALCAM
is asnp
is mentioned by
dbSNPrs1044243
ebirs1044243
HLIrs1044243
Exacrs1044243
Varsomers1044243
Maprs1044243
PheGenIrs1044243
hapmaprs1044243
1000 genomesrs1044243
hgdprs1044243
ensemblrs1044243
gopubmedrs1044243
geneviewrs1044243
scholarrs1044243
googlers1044243
pharmgkbrs1044243
gwascentralrs1044243
openSNPrs1044243
23andMers1044243
23andMe allrs1044243
SNP Nexus

SNPshotrs1044243
SNPdbers1044243
MSV3drs1044243
GWAS Ctlgrs1044243
GMAF0.06107
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21935604] Genetic variation in ALCAM and other chromosomal instability genes in breast cancer survival


GET Evidence
ALCAM-T301M
aa_change Thr301Met
aa_change_short T301M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0881205
summary