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rs104894306

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894306(C;T)
Make rs104894306(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position112087868
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs104894306
ebirs104894306
HLIrs104894306
Exacrs104894306
Varsomers104894306
Maprs104894306
PheGenIrs104894306
hapmaprs104894306
1000 genomesrs104894306
hgdprs104894306
ensemblrs104894306
gopubmedrs104894306
geneviewrs104894306
scholarrs104894306
googlers104894306
pharmgkbrs104894306
gwascentralrs104894306
openSNPrs104894306
23andMers104894306
23andMe allrs104894306
SNP Nexus

SNPshotrs104894306
SNPdbers104894306
MSV3drs104894306
GWAS Ctlgrs104894306
Max Magnitude0
OMIM602690
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104894306(T;T)
Alt rs104894306(T;T)
Reference rs104894306(C;C)
Significance Pathogenic
Disease Paragangliomas 1 Pheochromocytoma
Variation info
Gene TIMM8B SDHD
CLNDBN Paragangliomas 1 Pheochromocytoma
Reversed 0
HGVS NC_000011.9:g.111958592C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007312.2, RCV000193132.1,