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rs876658429

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658429(G;T)
Make rs876658429(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214752485
GeneBARD1
is asnp
is mentioned by
dbSNPrs876658429
ebirs876658429
HLIrs876658429
Exacrs876658429
Varsomers876658429
Maprs876658429
PheGenIrs876658429
hapmaprs876658429
1000 genomesrs876658429
hgdprs876658429
ensemblrs876658429
gopubmedrs876658429
geneviewrs876658429
scholarrs876658429
googlers876658429
pharmgkbrs876658429
gwascentralrs876658429
openSNPrs876658429
23andMers876658429
23andMe allrs876658429
SNP Nexus

SNPshotrs876658429
SNPdbers876658429
MSV3drs876658429
GWAS Ctlgrs876658429
Max Magnitude0
ClinVar
Risk rs876658429(T;T)
Alt rs876658429(T;T)
Reference rs876658429(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BARD1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000002.11:g.215617209C>A
CLNSRC
CLNACC RCV000213181.1,