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rs104894305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894305(A;A)
Make rs104894305(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position112087899
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs104894305
ebirs104894305
HLIrs104894305
Exacrs104894305
Varsomers104894305
Maprs104894305
PheGenIrs104894305
hapmaprs104894305
1000 genomesrs104894305
hgdprs104894305
ensemblrs104894305
gopubmedrs104894305
geneviewrs104894305
scholarrs104894305
googlers104894305
pharmgkbrs104894305
gwascentralrs104894305
openSNPrs104894305
23andMers104894305
23andMe allrs104894305
SNP Nexus

SNPshotrs104894305
SNPdbers104894305
MSV3drs104894305
GWAS Ctlgrs104894305
Max Magnitude0
OMIM602690
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894305(A;A)
Alt rs104894305(A;A)
Reference rs104894305(C;C)
Significance Pathogenic
Disease Paragangliomas 1
Variation info
Gene TIMM8B SDHD
CLNDBN Paragangliomas 1
Reversed 0
HGVS NC_000011.9:g.111958623C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007310.2,