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

rs74315371

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315371(A;A)
Make rs74315371(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position17028721
GeneSDHB
is asnp
is mentioned by
dbSNPrs74315371
ebirs74315371
HLIrs74315371
Exacrs74315371
Varsomers74315371
Maprs74315371
PheGenIrs74315371
hapmaprs74315371
1000 genomesrs74315371
hgdprs74315371
ensemblrs74315371
gopubmedrs74315371
geneviewrs74315371
scholarrs74315371
googlers74315371
pharmgkbrs74315371
gwascentralrs74315371
openSNPrs74315371
23andMers74315371
23andMe allrs74315371
SNP Nexus

SNPshotrs74315371
SNPdbers74315371
MSV3drs74315371
GWAS Ctlgrs74315371
Max Magnitude0
OMIM185470
Desc
Variant0009
Relatedalso
ClinVar
Risk rs74315371(A;A)
Alt rs74315371(A;A)
Reference rs74315371(G;G)
Significance Pathogenic
Disease Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17355216C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013627.24,