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rs878853995

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853995(C;G)
Make rs878853995(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214780702
GeneBARD1
is asnp
is mentioned by
dbSNPrs878853995
ebirs878853995
HLIrs878853995
Exacrs878853995
Varsomers878853995
Maprs878853995
PheGenIrs878853995
hapmaprs878853995
1000 genomesrs878853995
hgdprs878853995
ensemblrs878853995
gopubmedrs878853995
geneviewrs878853995
scholarrs878853995
googlers878853995
pharmgkbrs878853995
gwascentralrs878853995
openSNPrs878853995
23andMers878853995
23andMe allrs878853995
SNP Nexus

SNPshotrs878853995
SNPdbers878853995
MSV3drs878853995
GWAS Ctlgrs878853995
Max Magnitude0
ClinVar
Risk rs878853995(G;G)
Alt rs878853995(G;G)
Reference rs878853995(C;C)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BARD1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000002.11:g.215645426G>C
CLNSRC
CLNACC RCV000231412.1,