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rs876660219

From SNPedia

Orientationminus
Geno Mag Summary
(TTGTC;TTGTC) 0 common in clinvar
Make rs876660219(-;-)
Make rs876660219(-;TTGTC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61801291
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876660219
ebirs876660219
HLIrs876660219
Exacrs876660219
Varsomers876660219
Maprs876660219
PheGenIrs876660219
hapmaprs876660219
1000 genomesrs876660219
hgdprs876660219
ensemblrs876660219
gopubmedrs876660219
geneviewrs876660219
scholarrs876660219
googlers876660219
pharmgkbrs876660219
gwascentralrs876660219
openSNPrs876660219
23andMers876660219
23andMe allrs876660219
SNP Nexus

SNPshotrs876660219
SNPdbers876660219
MSV3drs876660219
GWAS Ctlgrs876660219
Max Magnitude0
ClinVar
Risk rs876660219(;)
Alt rs876660219(;)
Reference rs876660219(TTGTC;TTGTC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.59878652_59878656delGACAA
CLNSRC
CLNACC RCV000217387.1,