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

rs377153250

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377153250(C;C)
Make rs377153250(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214780658
GeneBARD1
is asnp
is mentioned by
dbSNPrs377153250
ebirs377153250
HLIrs377153250
Exacrs377153250
Varsomers377153250
Maprs377153250
PheGenIrs377153250
hapmaprs377153250
1000 genomesrs377153250
hgdprs377153250
ensemblrs377153250
gopubmedrs377153250
geneviewrs377153250
scholarrs377153250
googlers377153250
pharmgkbrs377153250
gwascentralrs377153250
openSNPrs377153250
23andMers377153250
23andMe allrs377153250
SNP Nexus

SNPshotrs377153250
SNPdbers377153250
MSV3drs377153250
GWAS Ctlgrs377153250
Max Magnitude0
ClinVar
Risk rs377153250(A,C;A,C)
Alt rs377153250(A,C;A,C)
Reference rs377153250(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BARD1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000002.11:g.215645382G>A; NC_000002.11:g.215645382G>C
CLNSRC
CLNACC RCV000217217.1, RCV000130569.4, RCV000212125.1,