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rs876659130

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659130(-;-)
Make rs876659130(-;A)
Make rs876659130(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position112087951
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs876659130
ebirs876659130
HLIrs876659130
Exacrs876659130
Varsomers876659130
Maprs876659130
PheGenIrs876659130
hapmaprs876659130
1000 genomesrs876659130
hgdprs876659130
ensemblrs876659130
gopubmedrs876659130
geneviewrs876659130
scholarrs876659130
googlers876659130
pharmgkbrs876659130
gwascentralrs876659130
openSNPrs876659130
23andMers876659130
23andMe allrs876659130
SNP Nexus

SNPshotrs876659130
SNPdbers876659130
MSV3drs876659130
GWAS Ctlgrs876659130
Max Magnitude0
ClinVar
Risk rs876659130(A;A)
Alt rs876659130(A;A)
Reference rs876659130(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TIMM8B SDHD
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.111958675dupA
CLNSRC
CLNACC RCV000217241.1,