Have questions? Visit https://www.reddit.com/r/SNPedia

rs80359198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80359198(C;G)
Make rs80359198(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394717
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359198
ebirs80359198
HLIrs80359198
Exacrs80359198
Varsomers80359198
Maprs80359198
PheGenIrs80359198
hapmaprs80359198
1000 genomesrs80359198
hgdprs80359198
ensemblrs80359198
gopubmedrs80359198
geneviewrs80359198
scholarrs80359198
googlers80359198
pharmgkbrs80359198
gwascentralrs80359198
openSNPrs80359198
23andMers80359198
23andMe allrs80359198
SNP Nexus

SNPshotrs80359198
SNPdbers80359198
MSV3drs80359198
GWAS Ctlgrs80359198
Max Magnitude0
ClinVar
Risk rs80359198(G,T;G,T)
Alt rs80359198(G,T;G,T)
Reference rs80359198(C;C)
Significance Other
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations not provided Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32968854C>A; NC_000013.10:g.32968854C>G; NC_000013.10:g.32968854C>T
CLNSRC ClinVar
CLNACC RCV000239130.1, RCV000045779.3, RCV000077467.4, RCV000223197.1, RCV000236007.1, RCV000164250.1, RCV000206162.1,