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rs730881411

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881411(C;T)
Make rs730881411(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214781426
GeneBARD1
is asnp
is mentioned by
dbSNPrs730881411
ebirs730881411
HLIrs730881411
Exacrs730881411
Varsomers730881411
Maprs730881411
PheGenIrs730881411
hapmaprs730881411
1000 genomesrs730881411
hgdprs730881411
ensemblrs730881411
gopubmedrs730881411
geneviewrs730881411
scholarrs730881411
googlers730881411
pharmgkbrs730881411
gwascentralrs730881411
openSNPrs730881411
23andMers730881411
23andMe allrs730881411
SNP Nexus

SNPshotrs730881411
SNPdbers730881411
MSV3drs730881411
GWAS Ctlgrs730881411
Max Magnitude0
ClinVar
Risk rs730881411(T;T)
Alt rs730881411(T;T)
Reference rs730881411(C;C)
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.215646150G>A
CLNSRC
CLNACC RCV000159805.2, RCV000213814.1,