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rs59004709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs59004709(A;A)
Make rs59004709(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379467
GeneBRCA2
is asnp
is mentioned by
dbSNPrs59004709
ClinGenrs59004709
ebirs59004709
HLIrs59004709
Exacrs59004709
Varsomers59004709
Maprs59004709
PheGenIrs59004709
hapmaprs59004709
1000 genomesrs59004709
hgdprs59004709
ensemblrs59004709
gopubmedrs59004709
geneviewrs59004709
scholarrs59004709
googlers59004709
pharmgkbrs59004709
gwascentralrs59004709
openSNPrs59004709
23andMers59004709
23andMe allrs59004709
SNP Nexus

SNPshotrs59004709
SNPdbers59004709
MSV3drs59004709
GWAS Ctlgrs59004709
GMAF0.001377
Max Magnitude0
ClinVar
Risk rs59004709(A;A)
Alt rs59004709(A;A)
Reference Rs59004709(G;G)
Significance Other
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32953604G>A
CLNSRC ClinVar Counsyl
CLNACC RCV000077456.6, RCV000163015.1, RCV000168609.4, RCV000195338.3,