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rs104894307

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs104894307(A;G)
Make rs104894307(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position112086908
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs104894307
ebirs104894307
HLIrs104894307
Exacrs104894307
Varsomers104894307
Maprs104894307
PheGenIrs104894307
hapmaprs104894307
1000 genomesrs104894307
hgdprs104894307
ensemblrs104894307
gopubmedrs104894307
geneviewrs104894307
scholarrs104894307
googlers104894307
pharmgkbrs104894307
gwascentralrs104894307
openSNPrs104894307
23andMers104894307
23andMe allrs104894307
SNP Nexus

SNPshotrs104894307
SNPdbers104894307
MSV3drs104894307
GWAS Ctlgrs104894307
Max Magnitude0
OMIM602690
Desc
Variant0021
Relatedalso
ClinVar
Risk rs104894307(G,T;G,T)
Alt rs104894307(G,T;G,T)
Reference rs104894307(A;A)
Significance Pathogenic
Disease Carotid body paraganglioma
Variation info
Gene TIMM8B SDHD
CLNDBN Carotid body paraganglioma
Reversed 0
HGVS NC_000011.9:g.111957632A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007320.4,