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rs398122753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122753(-;-)
Make rs398122753(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337163
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122753
ebirs398122753
HLIrs398122753
Exacrs398122753
Varsomers398122753
Maprs398122753
PheGenIrs398122753
hapmaprs398122753
1000 genomesrs398122753
hgdprs398122753
ensemblrs398122753
gopubmedrs398122753
geneviewrs398122753
scholarrs398122753
googlers398122753
pharmgkbrs398122753
gwascentralrs398122753
openSNPrs398122753
23andMers398122753
23andMe allrs398122753
SNP Nexus

SNPshotrs398122753
SNPdbers398122753
MSV3drs398122753
GWAS Ctlgrs398122753
Max Magnitude0
ClinVar
Risk rs398122753(;)
Alt rs398122753(;)
Reference rs398122753(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32911300delA
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000077695.2, RCV000129297.2, RCV000204896.1, RCV000218847.1,