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rs273901754

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;G) 6 BRCA1 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs273901754(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057051
GeneBRCA1
is asnp
is mentioned by
dbSNPrs273901754
ebirs273901754
HLIrs273901754
Exacrs273901754
Varsomers273901754
Maprs273901754
PheGenIrs273901754
hapmaprs273901754
1000 genomesrs273901754
hgdprs273901754
ensemblrs273901754
gopubmedrs273901754
geneviewrs273901754
scholarrs273901754
googlers273901754
pharmgkbrs273901754
gwascentralrs273901754
openSNPrs273901754
23andMers273901754
23andMe allrs273901754
SNP Nexus

SNPshotrs273901754
SNPdbers273901754
MSV3drs273901754
GWAS Ctlgrs273901754
Max Magnitude6
ClinVar
Risk
Alt
Reference Rs273901754(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.41209068delC
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000077161.4, RCV000164914.1, RCV000236858.1,