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rs151170408

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151170408(C;G)
Make rs151170408(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position235230
GeneSDHA
is asnp
is mentioned by
dbSNPrs151170408
ebirs151170408
HLIrs151170408
Exacrs151170408
Varsomers151170408
Maprs151170408
PheGenIrs151170408
hapmaprs151170408
1000 genomesrs151170408
hgdprs151170408
ensemblrs151170408
gopubmedrs151170408
geneviewrs151170408
scholarrs151170408
googlers151170408
pharmgkbrs151170408
gwascentralrs151170408
openSNPrs151170408
23andMers151170408
23andMe allrs151170408
SNP Nexus

SNPshotrs151170408
SNPdbers151170408
MSV3drs151170408
GWAS Ctlgrs151170408
Max Magnitude0
ClinVar
Risk rs151170408(G;G)
Alt rs151170408(G;G)
Reference rs151170408(C;C)
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.235345C>G
CLNSRC
CLNACC RCV000221764.1,