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rs876659491

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659491(-;-)
Make rs876659491(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17027847
GeneSDHB
is asnp
is mentioned by
dbSNPrs876659491
dbSNP (classic)rs876659491
ClinGenrs876659491
ebirs876659491
HLIrs876659491
Exacrs876659491
Gnomadrs876659491
Varsomers876659491
LitVarrs876659491
Maprs876659491
PheGenIrs876659491
Biobankrs876659491
1000 genomesrs876659491
hgdprs876659491
ensemblrs876659491
geneviewrs876659491
scholarrs876659491
googlers876659491
pharmgkbrs876659491
gwascentralrs876659491
openSNPrs876659491
23andMers876659491
SNPshotrs876659491
SNPdbers876659491
MSV3drs876659491
GWAS Ctlgrs876659491
Max Magnitude0
ClinVar
Risk rs876659491(-;-)
Alt rs876659491(-;-)
Reference Rs876659491(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17354342delC
CLNSRC
CLNACC RCV000220488.1,