Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658486

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658486(A;A)
Make rs876658486(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position226041
GeneSDHA
is asnp
is mentioned by
dbSNPrs876658486
ebirs876658486
HLIrs876658486
Exacrs876658486
Varsomers876658486
Maprs876658486
PheGenIrs876658486
hapmaprs876658486
1000 genomesrs876658486
hgdprs876658486
ensemblrs876658486
gopubmedrs876658486
geneviewrs876658486
scholarrs876658486
googlers876658486
pharmgkbrs876658486
gwascentralrs876658486
openSNPrs876658486
23andMers876658486
23andMe allrs876658486
SNP Nexus

SNPshotrs876658486
SNPdbers876658486
MSV3drs876658486
GWAS Ctlgrs876658486
Max Magnitude0
ClinVar
Risk rs876658486(A;A)
Alt rs876658486(A;A)
Reference rs876658486(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHA
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.226156T>A
CLNSRC
CLNACC RCV000221025.1,