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

rs138996609

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138996609(A;A)
Make rs138996609(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17022685
GeneSDHB
is asnp
is mentioned by
dbSNPrs138996609
ebirs138996609
HLIrs138996609
Exacrs138996609
Varsomers138996609
Maprs138996609
PheGenIrs138996609
hapmaprs138996609
1000 genomesrs138996609
hgdprs138996609
ensemblrs138996609
gopubmedrs138996609
geneviewrs138996609
scholarrs138996609
googlers138996609
pharmgkbrs138996609
gwascentralrs138996609
openSNPrs138996609
23andMers138996609
23andMe allrs138996609
SNP Nexus

SNPshotrs138996609
SNPdbers138996609
MSV3drs138996609
GWAS Ctlgrs138996609
Max Magnitude0
ClinVar
Risk rs138996609(A;A)
Alt rs138996609(A;A)
Reference rs138996609(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.17349180G>A
CLNSRC
CLNACC RCV000164435.1,