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rs752411477

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs752411477(A;G)
Make rs752411477(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61861516
GeneBRIP1
is asnp
is mentioned by
dbSNPrs752411477
ebirs752411477
HLIrs752411477
Exacrs752411477
Varsomers752411477
Maprs752411477
PheGenIrs752411477
hapmaprs752411477
1000 genomesrs752411477
hgdprs752411477
ensemblrs752411477
gopubmedrs752411477
geneviewrs752411477
scholarrs752411477
googlers752411477
pharmgkbrs752411477
gwascentralrs752411477
openSNPrs752411477
23andMers752411477
23andMe allrs752411477
SNP Nexus

SNPshotrs752411477
SNPdbers752411477
MSV3drs752411477
GWAS Ctlgrs752411477
Max Magnitude0
ClinVar
Risk rs752411477(G,T;G,T)
Alt rs752411477(G,T;G,T)
Reference rs752411477(A;A)
Significance 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.59938877A>T
CLNSRC
CLNACC RCV000216493.1,