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rs17468277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17468277(C;T)
Make rs17468277(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position201289477
GeneALS2CR12
is asnp
is mentioned by
dbSNPrs17468277
dbSNP (classic)rs17468277
ClinGenrs17468277
ebirs17468277
HLIrs17468277
Exacrs17468277
Gnomadrs17468277
Varsomers17468277
LitVarrs17468277
Maprs17468277
PheGenIrs17468277
Biobankrs17468277
1000 genomesrs17468277
hgdprs17468277
ensemblrs17468277
geneviewrs17468277
scholarrs17468277
googlers17468277
pharmgkbrs17468277
gwascentralrs17468277
openSNPrs17468277
23andMers17468277
SNPshotrs17468277
SNPdbers17468277
MSV3drs17468277
GWAS Ctlgrs17468277
GMAF0.06566
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20145138] Common genetic variants associated with breast cancer and mammographic density measures that predict disease


[PMID 21596841OA-icon.png] Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.


[PMID 22532573OA-icon.png] The role of genetic breast cancer susceptibility variants as prognostic factors.


[PMID 23479381] Breast cancer susceptibility loci in association with age at menarche, age at natural menopause and the reproductive lifespan


[PMID 23704029] Breast cancer susceptibility loci in association with age at menarche, age at natural menopause and the reproductive lifespan


ClinVar
Risk rs17468277(T;T)
Alt rs17468277(T;T)
Reference Rs17468277(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ALS2CR12
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.202154200C>T
CLNSRC
CLNACC RCV000455346.1,



[PMID 28757652OA-icon.png] Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study.