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rs690016541

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs690016541(-;-)
Make rs690016541(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337647
GeneBRCA2
is asnp
is mentioned by
dbSNPrs690016541
ebirs690016541
HLIrs690016541
Exacrs690016541
Varsomers690016541
Maprs690016541
PheGenIrs690016541
hapmaprs690016541
1000 genomesrs690016541
hgdprs690016541
ensemblrs690016541
gopubmedrs690016541
geneviewrs690016541
scholarrs690016541
googlers690016541
pharmgkbrs690016541
gwascentralrs690016541
openSNPrs690016541
23andMers690016541
23andMe allrs690016541
SNP Nexus

SNPshotrs690016541
SNPdbers690016541
MSV3drs690016541
GWAS Ctlgrs690016541
Max Magnitude0
ClinVar
Risk rs690016541(;)
Alt rs690016541(;)
Reference rs690016541(A;A)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911784delA
CLNSRC VariO
CLNACC RCV000149514.1,