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rs690016539

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs690016539(A;T)
Make rs690016539(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337635
GeneBRCA2
is asnp
is mentioned by
dbSNPrs690016539
ebirs690016539
HLIrs690016539
Exacrs690016539
Varsomers690016539
Maprs690016539
PheGenIrs690016539
hapmaprs690016539
1000 genomesrs690016539
hgdprs690016539
ensemblrs690016539
gopubmedrs690016539
geneviewrs690016539
scholarrs690016539
googlers690016539
pharmgkbrs690016539
gwascentralrs690016539
openSNPrs690016539
23andMers690016539
23andMe allrs690016539
SNP Nexus

SNPshotrs690016539
SNPdbers690016539
MSV3drs690016539
GWAS Ctlgrs690016539
Max Magnitude0
ClinVar
Risk rs690016539(T;T)
Alt rs690016539(T;T)
Reference rs690016539(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.32911772A>T
CLNSRC VariO
CLNACC RCV000149512.1,