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rs9397435

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs9397435(A;G)
Make rs9397435(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position151630085
is asnp
is mentioned by
dbSNPrs9397435
ebirs9397435
HLIrs9397435
Exacrs9397435
Varsomers9397435
Maprs9397435
PheGenIrs9397435
hapmaprs9397435
1000 genomesrs9397435
hgdprs9397435
ensemblrs9397435
gopubmedrs9397435
geneviewrs9397435
scholarrs9397435
googlers9397435
pharmgkbrs9397435
gwascentralrs9397435
openSNPrs9397435
23andMers9397435
23andMe allrs9397435
SNP Nexus

SNPshotrs9397435
SNPdbers9397435
MSV3drs9397435
GWAS Ctlgrs9397435
GMAF0.1189
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20661439OA-icon.png] Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus

[PMID 21593217OA-icon.png] Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

[PMID 22357627OA-icon.png] Evaluation of 19 Susceptibility Loci of Breast Cancer in Women of African Ancestry

ClinVar
Risk rs9397435(G;G)
Alt rs9397435(G;G)
Reference rs9397435(A;A)
Significance Other
Disease Estrogen resistance
Variation info
Gene LOC105378058
CLNDBN Estrogen resistance
Reversed 0
HGVS NC_000006.12:g.151630085A>G
CLNSRC
CLNACC RCV000143995.1,