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rs397514034

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs397514034(-;-)
Make rs397514034(-;TC)
ReferenceGRCh38 38.1/141
Chromosome11
Position112087898
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs397514034
ebirs397514034
HLIrs397514034
Exacrs397514034
Varsomers397514034
Maprs397514034
PheGenIrs397514034
hapmaprs397514034
1000 genomesrs397514034
hgdprs397514034
ensemblrs397514034
gopubmedrs397514034
geneviewrs397514034
scholarrs397514034
googlers397514034
pharmgkbrs397514034
gwascentralrs397514034
openSNPrs397514034
23andMers397514034
23andMe allrs397514034
SNP Nexus

SNPshotrs397514034
SNPdbers397514034
MSV3drs397514034
GWAS Ctlgrs397514034
Max Magnitude0
ClinVar
Risk rs397514034(;)
Alt rs397514034(;)
Reference rs397514034(TC;TC)
Significance Pathogenic
Disease Paragangliomas 1
Variation info
Gene TIMM8B SDHD
CLNDBN Paragangliomas 1
Reversed 0
HGVS NC_000011.9:g.111958622_111958623delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007317.2,