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rs55763607

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55763607(C;T)
Make rs55763607(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32370490
GeneBRCA2
is asnp
is mentioned by
dbSNPrs55763607
ebirs55763607
HLIrs55763607
Exacrs55763607
Varsomers55763607
Maprs55763607
PheGenIrs55763607
hapmaprs55763607
1000 genomesrs55763607
hgdprs55763607
ensemblrs55763607
gopubmedrs55763607
geneviewrs55763607
scholarrs55763607
googlers55763607
pharmgkbrs55763607
gwascentralrs55763607
openSNPrs55763607
23andMers55763607
23andMe allrs55763607
SNP Nexus

SNPshotrs55763607
SNPdbers55763607
MSV3drs55763607
GWAS Ctlgrs55763607
Max Magnitude0
ClinVar
Risk rs55763607(T;T)
Alt rs55763607(T;T)
Reference rs55763607(C;C)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32944627C>A; NC_000013.10:g.32944627C>T
CLNSRC
CLNACC RCV000196106.2, RCV000045513.4, RCV000083147.3, RCV000130247.2, RCV000212274.1,