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rs1060502395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502395(-;-)
Make rs1060502395(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32326146
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502395
dbSNP (old)rs1060502395
ClinGenrs1060502395
ebirs1060502395
HLIrs1060502395
Exacrs1060502395
Gnomadrs1060502395
Varsomers1060502395
LitVarrs1060502395
Maprs1060502395
PheGenIrs1060502395
Biobankrs1060502395
1000 genomesrs1060502395
hgdprs1060502395
ensemblrs1060502395
gopubmedrs1060502395
geneviewrs1060502395
scholarrs1060502395
googlers1060502395
pharmgkbrs1060502395
gwascentralrs1060502395
openSNPrs1060502395
23andMers1060502395
23andMe allrs1060502395
SNPshotrs1060502395
SNPdbers1060502395
MSV3drs1060502395
GWAS Ctlgrs1060502395
Max Magnitude0
ClinVar
Risk rs1060502395(-;-)
Alt rs1060502395(-;-)
Reference Rs1060502395(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.32900283delG
CLNSRC
CLNACC RCV000461133.1,