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rs587779349

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779349(-;-)
Make rs587779349(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32380041
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587779349
ebirs587779349
HLIrs587779349
Exacrs587779349
Varsomers587779349
Maprs587779349
PheGenIrs587779349
hapmaprs587779349
1000 genomesrs587779349
hgdprs587779349
ensemblrs587779349
gopubmedrs587779349
geneviewrs587779349
scholarrs587779349
googlers587779349
pharmgkbrs587779349
gwascentralrs587779349
openSNPrs587779349
23andMers587779349
23andMe allrs587779349
SNP Nexus

SNPshotrs587779349
SNPdbers587779349
MSV3drs587779349
GWAS Ctlgrs587779349
Max Magnitude0
ClinVar
Risk rs587779349(;)
Alt rs587779349(;)
Reference rs587779349(C;C)
Significance Pathogenic
Disease Ateleiotic dwarfism
Variation info
Gene BRCA2
CLNDBN Ateleiotic dwarfism
Reversed 0
HGVS NC_000013.10:g.32954178delC
CLNSRC VariO
CLNACC RCV000115039.1,