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rs80357299

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80357299(A;C)
Make rs80357299(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045749
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357299
ebirs80357299
HLIrs80357299
Exacrs80357299
Varsomers80357299
Maprs80357299
PheGenIrs80357299
hapmaprs80357299
1000 genomesrs80357299
hgdprs80357299
ensemblrs80357299
gopubmedrs80357299
geneviewrs80357299
scholarrs80357299
googlers80357299
pharmgkbrs80357299
gwascentralrs80357299
openSNPrs80357299
23andMers80357299
23andMe allrs80357299
SNP Nexus

SNPshotrs80357299
SNPdbers80357299
MSV3drs80357299
GWAS Ctlgrs80357299
Max Magnitude0
ClinVar
Risk rs80357299(C;C)
Alt rs80357299(C;C)
Reference rs80357299(A;A)
Significance Untested
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41197766T>G
CLNSRC ClinVar
CLNACC RCV000031262.4, RCV000049033.2,