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rs398122618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122618(-;-)
Make rs398122618(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398195
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122618
ebirs398122618
HLIrs398122618
Exacrs398122618
Varsomers398122618
Maprs398122618
PheGenIrs398122618
hapmaprs398122618
1000 genomesrs398122618
hgdprs398122618
ensemblrs398122618
gopubmedrs398122618
geneviewrs398122618
scholarrs398122618
googlers398122618
pharmgkbrs398122618
gwascentralrs398122618
openSNPrs398122618
23andMers398122618
23andMe allrs398122618
SNP Nexus

SNPshotrs398122618
SNPdbers398122618
MSV3drs398122618
GWAS Ctlgrs398122618
Max Magnitude0
ClinVar
Risk rs398122618(;)
Alt rs398122618(;)
Reference rs398122618(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32972332delA
CLNSRC ClinVar
CLNACC RCV000077047.2,