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rs776851287

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776851287(A;A)
Make rs776851287(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position214781348
GeneBARD1
is asnp
is mentioned by
dbSNPrs776851287
dbSNP (old)rs776851287
ClinGenrs776851287
ebirs776851287
HLIrs776851287
Exacrs776851287
Gnomadrs776851287
Varsomers776851287
Maprs776851287
PheGenIrs776851287
Biobankrs776851287
1000 genomesrs776851287
hgdprs776851287
ensemblrs776851287
gopubmedrs776851287
geneviewrs776851287
scholarrs776851287
googlers776851287
pharmgkbrs776851287
gwascentralrs776851287
openSNPrs776851287
23andMers776851287
23andMe allrs776851287
SNPshotrs776851287
SNPdbers776851287
MSV3drs776851287
GWAS Ctlgrs776851287
Max Magnitude0
ClinVar
Risk rs776851287(A;A)
Alt rs776851287(A;A)
Reference Rs776851287(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BARD1
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000002.11:g.215646072G>A
CLNSRC
CLNACC RCV000462626.1,