Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781804

From SNPedia

Orientationplus
Geno Mag Summary
(TCAT;TCAT) 0 common in clinvar
Make rs587781804(-;-)
Make rs587781804(-;TCAT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32332906
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781804
ebirs587781804
HLIrs587781804
Exacrs587781804
Varsomers587781804
Maprs587781804
PheGenIrs587781804
hapmaprs587781804
1000 genomesrs587781804
hgdprs587781804
ensemblrs587781804
gopubmedrs587781804
geneviewrs587781804
scholarrs587781804
googlers587781804
pharmgkbrs587781804
gwascentralrs587781804
openSNPrs587781804
23andMers587781804
23andMe allrs587781804
SNP Nexus

SNPshotrs587781804
SNPdbers587781804
MSV3drs587781804
GWAS Ctlgrs587781804
Max Magnitude0
ClinVar
Risk rs587781804(;)
Alt rs587781804(;)
Reference rs587781804(TCAT;TCAT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32907043_32907046delTCAT
CLNSRC
CLNACC RCV000130073.2,