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rs886041237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome11
Position112087857
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs886041237
dbSNP (classic)rs886041237
ClinGenrs886041237
ebirs886041237
HLIrs886041237
Exacrs886041237
Gnomadrs886041237
Varsomers886041237
LitVarrs886041237
Maprs886041237
PheGenIrs886041237
Biobankrs886041237
1000 genomesrs886041237
hgdprs886041237
ensemblrs886041237
geneviewrs886041237
scholarrs886041237
googlers886041237
pharmgkbrs886041237
gwascentralrs886041237
openSNPrs886041237
23andMers886041237
23andMe allrs886041237
SNPshotrs886041237
SNPdbers886041237
MSV3drs886041237
GWAS Ctlgrs886041237
Max Magnitude0
ClinVar
Risk rs886041237(C;C)
Alt rs886041237(C;C)
Reference Rs886041237(-;-)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene TIMM8B SDHD
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.111958581dupC
CLNSRC
CLNACC RCV000349345.1, RCV000492278.1,