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rs80358033

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80358033(A;C)
Make rs80358033(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43095924
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358033
ebirs80358033
HLIrs80358033
Exacrs80358033
Varsomers80358033
Maprs80358033
PheGenIrs80358033
hapmaprs80358033
1000 genomesrs80358033
hgdprs80358033
ensemblrs80358033
gopubmedrs80358033
geneviewrs80358033
scholarrs80358033
googlers80358033
pharmgkbrs80358033
gwascentralrs80358033
openSNPrs80358033
23andMers80358033
23andMe allrs80358033
SNP Nexus

SNPshotrs80358033
SNPdbers80358033
MSV3drs80358033
GWAS Ctlgrs80358033
Max Magnitude0
ClinVar
Risk rs80358033(C,G;C,G)
Alt rs80358033(C,G;C,G)
Reference rs80358033(A;A)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.41247941T>C; NC_000017.10:g.41247941T>G
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000049068.2, RCV000031267.8, RCV000049067.4, RCV000131863.2, RCV000159940.3, RCV000225499.1,