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rs876660237

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660237(G;T)
Make rs876660237(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214745066
GeneBARD1
is asnp
is mentioned by
dbSNPrs876660237
ebirs876660237
HLIrs876660237
Exacrs876660237
Varsomers876660237
Maprs876660237
PheGenIrs876660237
hapmaprs876660237
1000 genomesrs876660237
hgdprs876660237
ensemblrs876660237
gopubmedrs876660237
geneviewrs876660237
scholarrs876660237
googlers876660237
pharmgkbrs876660237
gwascentralrs876660237
openSNPrs876660237
23andMers876660237
23andMe allrs876660237
SNP Nexus

SNPshotrs876660237
SNPdbers876660237
MSV3drs876660237
GWAS Ctlgrs876660237
Max Magnitude0
ClinVar
Risk rs876660237(T;T)
Alt rs876660237(T;T)
Reference rs876660237(G;G)
Significance Probable-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.215609790C>A
CLNSRC
CLNACC RCV000220803.1,