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rs690016542

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016542(-;-)
Make rs690016542(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337996
GeneBRCA2
is asnp
is mentioned by
dbSNPrs690016542
ebirs690016542
HLIrs690016542
Exacrs690016542
Varsomers690016542
Maprs690016542
PheGenIrs690016542
hapmaprs690016542
1000 genomesrs690016542
hgdprs690016542
ensemblrs690016542
gopubmedrs690016542
geneviewrs690016542
scholarrs690016542
googlers690016542
pharmgkbrs690016542
gwascentralrs690016542
openSNPrs690016542
23andMers690016542
23andMe allrs690016542
SNP Nexus

SNPshotrs690016542
SNPdbers690016542
MSV3drs690016542
GWAS Ctlgrs690016542
Max Magnitude0
ClinVar
Risk rs690016542(;)
Alt rs690016542(;)
Reference rs690016542(T;T)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912133delT
CLNSRC VariO
CLNACC RCV000149515.1,