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rs876660203

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660203(A;A)
Make rs876660203(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61685835
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876660203
ebirs876660203
HLIrs876660203
Exacrs876660203
Varsomers876660203
Maprs876660203
PheGenIrs876660203
hapmaprs876660203
1000 genomesrs876660203
hgdprs876660203
ensemblrs876660203
gopubmedrs876660203
geneviewrs876660203
scholarrs876660203
googlers876660203
pharmgkbrs876660203
gwascentralrs876660203
openSNPrs876660203
23andMers876660203
23andMe allrs876660203
SNP Nexus

SNPshotrs876660203
SNPdbers876660203
MSV3drs876660203
GWAS Ctlgrs876660203
Max Magnitude0
ClinVar
Risk rs876660203(A;A)
Alt rs876660203(A;A)
Reference rs876660203(G;G)
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.59763196C>T
CLNSRC
CLNACC RCV000216911.1,