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

rs587781270

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781270(A;A)
Make rs587781270(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17033058
GeneSDHB
is asnp
is mentioned by
dbSNPrs587781270
ebirs587781270
HLIrs587781270
Exacrs587781270
Varsomers587781270
Maprs587781270
PheGenIrs587781270
hapmaprs587781270
1000 genomesrs587781270
hgdprs587781270
ensemblrs587781270
gopubmedrs587781270
geneviewrs587781270
scholarrs587781270
googlers587781270
pharmgkbrs587781270
gwascentralrs587781270
openSNPrs587781270
23andMers587781270
23andMe allrs587781270
SNP Nexus

SNPshotrs587781270
SNPdbers587781270
MSV3drs587781270
GWAS Ctlgrs587781270
Max Magnitude0
ClinVar
Risk rs587781270(A;A)
Alt rs587781270(A;A)
Reference rs587781270(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17359553A>T
CLNSRC
CLNACC RCV000128905.2,