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

rs587781422

From SNPedia

Orientationplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs587781422(GG;TA)
Make rs587781422(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32380145
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781422
ebirs587781422
HLIrs587781422
Exacrs587781422
Varsomers587781422
Maprs587781422
PheGenIrs587781422
hapmaprs587781422
1000 genomesrs587781422
hgdprs587781422
ensemblrs587781422
gopubmedrs587781422
geneviewrs587781422
scholarrs587781422
googlers587781422
pharmgkbrs587781422
gwascentralrs587781422
openSNPrs587781422
23andMers587781422
23andMe allrs587781422
SNP Nexus

SNPshotrs587781422
SNPdbers587781422
MSV3drs587781422
GWAS Ctlgrs587781422
Max Magnitude0
ClinVar
Risk rs587781422(TA;TA)
Alt rs587781422(TA;TA)
Reference rs587781422(GG;GG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32954282_32954283delGGinsTA
CLNSRC
CLNACC RCV000129299.2,