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rs876659988

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659988(A;GTTCATAGCGG)
Make rs876659988(GTTCATAGCGG;GTTCATAGCGG)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position86919187
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs876659988
ebirs876659988
HLIrs876659988
Exacrs876659988
Varsomers876659988
Maprs876659988
PheGenIrs876659988
hapmaprs876659988
1000 genomesrs876659988
hgdprs876659988
ensemblrs876659988
gopubmedrs876659988
geneviewrs876659988
scholarrs876659988
googlers876659988
pharmgkbrs876659988
gwascentralrs876659988
openSNPrs876659988
23andMers876659988
23andMe allrs876659988
SNP Nexus

SNPshotrs876659988
SNPdbers876659988
MSV3drs876659988
GWAS Ctlgrs876659988
Max Magnitude0
ClinVar
Risk rs876659988(GTTCATAGCGG;GTTCATAGCGG)
Alt rs876659988(GTTCATAGCGG;GTTCATAGCGG)
Reference rs876659988(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BMPR1A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.88678944delAinsGTTCATAGCGG
CLNSRC
CLNACC RCV000222176.1,