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rs55933907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs55933907(A;A)
Make rs55933907(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380124
GeneBRCA2
is asnp
is mentioned by
dbSNPrs55933907
ebirs55933907
HLIrs55933907
Exacrs55933907
Varsomers55933907
Maprs55933907
PheGenIrs55933907
hapmaprs55933907
1000 genomesrs55933907
hgdprs55933907
ensemblrs55933907
gopubmedrs55933907
geneviewrs55933907
scholarrs55933907
googlers55933907
pharmgkbrs55933907
gwascentralrs55933907
openSNPrs55933907
23andMers55933907
23andMe allrs55933907
SNP Nexus

SNPshotrs55933907
SNPdbers55933907
MSV3drs55933907
GWAS Ctlgrs55933907
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs55933907(A;A)
Alt rs55933907(A;A)
Reference rs55933907(G;G)
Significance Other
Disease Breast-ovarian cancer not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32954261G>A
CLNSRC ClinVar
CLNACC RCV000031803.8, RCV000120369.2, RCV000162558.1, RCV000167789.4, RCV000176450.1,