Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881422

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881422(C;T)
Make rs730881422(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214730416
GeneBARD1
is asnp
is mentioned by
dbSNPrs730881422
ebirs730881422
HLIrs730881422
Exacrs730881422
Varsomers730881422
Maprs730881422
PheGenIrs730881422
hapmaprs730881422
1000 genomesrs730881422
hgdprs730881422
ensemblrs730881422
gopubmedrs730881422
geneviewrs730881422
scholarrs730881422
googlers730881422
pharmgkbrs730881422
gwascentralrs730881422
openSNPrs730881422
23andMers730881422
23andMe allrs730881422
SNP Nexus

SNPshotrs730881422
SNPdbers730881422
MSV3drs730881422
GWAS Ctlgrs730881422
Max Magnitude0
ClinVar
Risk rs730881422(T;T)
Alt rs730881422(T;T)
Reference rs730881422(C;C)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Variation info
Gene BARD1
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Reversed 1
HGVS NC_000002.11:g.215595140G>A
CLNSRC
CLNACC RCV000159820.2, RCV000222541.1, RCV000225939.1,