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rs1078806

From SNPedia

Orientationminus
Stabilizedminus
Make rs1078806(C;C)
Make rs1078806(C;T)
Make rs1078806(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position121579461
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1078806
ebirs1078806
HLIrs1078806
Exacrs1078806
Varsomers1078806
Maprs1078806
PheGenIrs1078806
hapmaprs1078806
1000 genomesrs1078806
hgdprs1078806
ensemblrs1078806
gopubmedrs1078806
geneviewrs1078806
scholarrs1078806
googlers1078806
pharmgkbrs1078806
gwascentralrs1078806
openSNPrs1078806
23andMers1078806
23andMe allrs1078806
SNP Nexus

SNPshotrs1078806
SNPdbers1078806
MSV3drs1078806
GWAS Ctlgrs1078806
GMAF0.3343
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21382839OA-icon.png] Relation of FGFR2 Genetic Polymorphisms to the Association Between Oral Contraceptive Use and the Risk of Breast Cancer in Chinese Women


[PMID 18326623OA-icon.png] Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.


[PMID 19738052OA-icon.png] A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.

GWAS snp
PMID [PMID 23354978OA-icon.png]
Trait Breast cancer
Title Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.
Risk Allele C
P-val 2E-6
Odds Ratio 1.43 [NR]