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rs876658301

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658301(-;-)
Make rs876658301(-;T)
Make rs876658301(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position161356811
GeneSDHC
is asnp
is mentioned by
dbSNPrs876658301
ebirs876658301
HLIrs876658301
Exacrs876658301
Varsomers876658301
Maprs876658301
PheGenIrs876658301
hapmaprs876658301
1000 genomesrs876658301
hgdprs876658301
ensemblrs876658301
gopubmedrs876658301
geneviewrs876658301
scholarrs876658301
googlers876658301
pharmgkbrs876658301
gwascentralrs876658301
openSNPrs876658301
23andMers876658301
23andMe allrs876658301
SNP Nexus

SNPshotrs876658301
SNPdbers876658301
MSV3drs876658301
GWAS Ctlgrs876658301
Max Magnitude0
ClinVar
Risk rs876658301(T;T)
Alt rs876658301(T;T)
Reference rs876658301(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHC
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000001.10:g.161326601dupT
CLNSRC
CLNACC RCV000215996.1,