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rs730881613

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881613(-;-)
Make rs730881613(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32356580
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881613
ebirs730881613
HLIrs730881613
Exacrs730881613
Varsomers730881613
Maprs730881613
PheGenIrs730881613
hapmaprs730881613
1000 genomesrs730881613
hgdprs730881613
ensemblrs730881613
gopubmedrs730881613
geneviewrs730881613
scholarrs730881613
googlers730881613
pharmgkbrs730881613
gwascentralrs730881613
openSNPrs730881613
23andMers730881613
23andMe allrs730881613
SNP Nexus

SNPshotrs730881613
SNPdbers730881613
MSV3drs730881613
GWAS Ctlgrs730881613
Max Magnitude0
ClinVar
Risk rs730881613(;)
Alt rs730881613(;)
Reference rs730881613(C;C)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32930717delC
CLNSRC
CLNACC RCV000160305.1,