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rs876659276

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659276(A;A)
Make rs876659276(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position112094830
GeneSDHD
is asnp
is mentioned by
dbSNPrs876659276
ebirs876659276
HLIrs876659276
Exacrs876659276
Varsomers876659276
Maprs876659276
PheGenIrs876659276
hapmaprs876659276
1000 genomesrs876659276
hgdprs876659276
ensemblrs876659276
gopubmedrs876659276
geneviewrs876659276
scholarrs876659276
googlers876659276
pharmgkbrs876659276
gwascentralrs876659276
openSNPrs876659276
23andMers876659276
23andMe allrs876659276
SNP Nexus

SNPshotrs876659276
SNPdbers876659276
MSV3drs876659276
GWAS Ctlgrs876659276
Max Magnitude0
ClinVar
Risk rs876659276(A;A)
Alt rs876659276(A;A)
Reference rs876659276(T;T)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHD
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.111965554T>A
CLNSRC
CLNACC RCV000215839.1,