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rs876660100

From SNPedia

Orientationminus
Geno Mag Summary
(TGATCCTGAA;TGATCCTGAA) 0 common in clinvar
Make rs876660100(-;-)
Make rs876660100(-;TGATCCTGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61683626
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876660100
ebirs876660100
HLIrs876660100
Exacrs876660100
Varsomers876660100
Maprs876660100
PheGenIrs876660100
hapmaprs876660100
1000 genomesrs876660100
hgdprs876660100
ensemblrs876660100
gopubmedrs876660100
geneviewrs876660100
scholarrs876660100
googlers876660100
pharmgkbrs876660100
gwascentralrs876660100
openSNPrs876660100
23andMers876660100
23andMe allrs876660100
SNP Nexus

SNPshotrs876660100
SNPdbers876660100
MSV3drs876660100
GWAS Ctlgrs876660100
Max Magnitude0
ClinVar
Risk rs876660100(;)
Alt rs876660100(;)
Reference rs876660100(TGATCCTGAA;TGATCCTGAA)
Significance Probable-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.59760987_59760996delTTCAGGATCA
CLNSRC
CLNACC RCV000213148.1,