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rs772486760

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs772486760(-;-)
Make rs772486760(-;TTTC)
Make rs772486760(TTTC;TTTC)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214781413
GeneBARD1
is asnp
is mentioned by
dbSNPrs772486760
ebirs772486760
HLIrs772486760
Exacrs772486760
Varsomers772486760
Maprs772486760
PheGenIrs772486760
hapmaprs772486760
1000 genomesrs772486760
hgdprs772486760
ensemblrs772486760
gopubmedrs772486760
geneviewrs772486760
scholarrs772486760
googlers772486760
pharmgkbrs772486760
gwascentralrs772486760
openSNPrs772486760
23andMers772486760
23andMe allrs772486760
SNP Nexus

SNPshotrs772486760
SNPdbers772486760
MSV3drs772486760
GWAS Ctlgrs772486760
Max Magnitude0
ClinVar
Risk rs772486760(CTTT;CTTT)
Alt rs772486760(CTTT;CTTT)
Reference rs772486760(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BARD1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.215646138_215646141dupCTTT
CLNSRC
CLNACC RCV000220804.1,