rs17468277

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs17468277(C;T)

Make rs17468277(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

201289477

Gene

ALS2CR12

is a	snp
is	mentioned by
dbSNP	rs17468277
dbSNP (classic)	rs17468277
ClinGen	rs17468277
ebi	rs17468277
HLI	rs17468277
Exac	rs17468277
Gnomad	rs17468277
Varsome	rs17468277
LitVar	rs17468277
Map	rs17468277
PheGenI	rs17468277
Biobank	rs17468277
1000 genomes	rs17468277
hgdp	rs17468277
ensembl	rs17468277
geneview	rs17468277
scholar	rs17468277
google	rs17468277
pharmgkb	rs17468277
gwascentral	rs17468277
openSNP	rs17468277
23andMe	rs17468277
SNPshot	rs17468277
SNPdbe	rs17468277
MSV3d	rs17468277
GWAS Ctlg	rs17468277

GMAF

0.06566

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

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

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

[PMID 22532573 ] 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 28757652 ] Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study.