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rs771654971

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs771654971(-;-)
Make rs771654971(-;T)
Make rs771654971(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61683785
GeneBRIP1
is asnp
is mentioned by
dbSNPrs771654971
ebirs771654971
HLIrs771654971
Exacrs771654971
Varsomers771654971
Maprs771654971
PheGenIrs771654971
hapmaprs771654971
1000 genomesrs771654971
hgdprs771654971
ensemblrs771654971
gopubmedrs771654971
geneviewrs771654971
scholarrs771654971
googlers771654971
pharmgkbrs771654971
gwascentralrs771654971
openSNPrs771654971
23andMers771654971
23andMe allrs771654971
SNP Nexus

SNPshotrs771654971
SNPdbers771654971
MSV3drs771654971
GWAS Ctlgrs771654971
Max Magnitude0
ClinVar
Risk rs771654971(T;T)
Alt rs771654971(T;T)
Reference rs771654971(;)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.59761147dupT
CLNSRC
CLNACC RCV000219598.1,