Have questions? Visit https://www.reddit.com/r/SNPedia

rs121917755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917755(C;T)
Make rs121917755(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position17028724
GeneSDHB
is asnp
is mentioned by
dbSNPrs121917755
ebirs121917755
HLIrs121917755
Exacrs121917755
Varsomers121917755
Maprs121917755
PheGenIrs121917755
hapmaprs121917755
1000 genomesrs121917755
hgdprs121917755
ensemblrs121917755
gopubmedrs121917755
geneviewrs121917755
scholarrs121917755
googlers121917755
pharmgkbrs121917755
gwascentralrs121917755
openSNPrs121917755
23andMers121917755
23andMe allrs121917755
SNP Nexus

SNPshotrs121917755
SNPdbers121917755
MSV3drs121917755
GWAS Ctlgrs121917755
Max Magnitude0
OMIM185470
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121917755(T;T)
Alt rs121917755(T;T)
Reference rs121917755(C;C)
Significance Pathogenic
Disease Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17355219G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013629.24,