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

rs1060502449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502449(G;T)
Make rs1060502449(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32337461
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502449
dbSNP (classic)rs1060502449
ClinGenrs1060502449
ebirs1060502449
HLIrs1060502449
Exacrs1060502449
Gnomadrs1060502449
Varsomers1060502449
LitVarrs1060502449
Maprs1060502449
PheGenIrs1060502449
Biobankrs1060502449
1000 genomesrs1060502449
hgdprs1060502449
ensemblrs1060502449
geneviewrs1060502449
scholarrs1060502449
googlers1060502449
pharmgkbrs1060502449
gwascentralrs1060502449
openSNPrs1060502449
23andMers1060502449
23andMe allrs1060502449
SNPshotrs1060502449
SNPdbers1060502449
MSV3drs1060502449
GWAS Ctlgrs1060502449
Max Magnitude0
ClinVar
Risk rs1060502449(T;T)
Alt rs1060502449(T;T)
Reference Rs1060502449(G;G)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32911598G>T
CLNSRC
CLNACC RCV000456163.1,