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rs730881415

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881415(G;T)
Make rs730881415(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214781267
GeneBARD1
is asnp
is mentioned by
dbSNPrs730881415
ebirs730881415
HLIrs730881415
Exacrs730881415
Varsomers730881415
Maprs730881415
PheGenIrs730881415
hapmaprs730881415
1000 genomesrs730881415
hgdprs730881415
ensemblrs730881415
gopubmedrs730881415
geneviewrs730881415
scholarrs730881415
googlers730881415
pharmgkbrs730881415
gwascentralrs730881415
openSNPrs730881415
23andMers730881415
23andMe allrs730881415
SNP Nexus

SNPshotrs730881415
SNPdbers730881415
MSV3drs730881415
GWAS Ctlgrs730881415
Max Magnitude0
ClinVar
Risk rs730881415(A,T;A,T)
Alt rs730881415(A,T;A,T)
Reference rs730881415(G;G)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BARD1
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000002.11:g.215645991C>A; NC_000002.11:g.215645991C>T
CLNSRC
CLNACC RCV000159811.1, RCV000216447.1,