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rs876660368

From SNPedia

Orientationminus
Geno Mag Summary
(GGTGAGG;GGTGAGG) 0 common in clinvar
Make rs876660368(-;-)
Make rs876660368(-;GGTGAGG)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17023967
GeneSDHB
is asnp
is mentioned by
dbSNPrs876660368
ebirs876660368
HLIrs876660368
Exacrs876660368
Varsomers876660368
Maprs876660368
PheGenIrs876660368
hapmaprs876660368
1000 genomesrs876660368
hgdprs876660368
ensemblrs876660368
gopubmedrs876660368
geneviewrs876660368
scholarrs876660368
googlers876660368
pharmgkbrs876660368
gwascentralrs876660368
openSNPrs876660368
23andMers876660368
23andMe allrs876660368
SNP Nexus

SNPshotrs876660368
SNPdbers876660368
MSV3drs876660368
GWAS Ctlgrs876660368
Max Magnitude0
ClinVar
Risk rs876660368(;)
Alt rs876660368(;)
Reference rs876660368(GGTGAGG;GGTGAGG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHB
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.17350462_17350468delCCTCACC
CLNSRC
CLNACC RCV000215647.1,