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rs398123690

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123690(-;-)
Make rs398123690(-;CC)
Make rs398123690(CC;CC)
ReferenceGRCh38 38.1/141
Chromosome1
Position17044848
GeneSDHB
is asnp
is mentioned by
dbSNPrs398123690
ebirs398123690
HLIrs398123690
Exacrs398123690
Varsomers398123690
Maprs398123690
PheGenIrs398123690
hapmaprs398123690
1000 genomesrs398123690
hgdprs398123690
ensemblrs398123690
gopubmedrs398123690
geneviewrs398123690
scholarrs398123690
googlers398123690
pharmgkbrs398123690
gwascentralrs398123690
openSNPrs398123690
23andMers398123690
23andMe allrs398123690
SNP Nexus

SNPshotrs398123690
SNPdbers398123690
MSV3drs398123690
GWAS Ctlgrs398123690
Max Magnitude0
ClinVar
Risk rs398123690(CC;CC)
Alt rs398123690(CC;CC)
Reference rs398123690(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SDHB
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.17371344_17371345dupGG
CLNSRC ClinVar
CLNACC RCV000080042.3,