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rs981049067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs981049067(C;C)
Make rs981049067(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position161356822
GeneSDHC
is asnp
is mentioned by
dbSNPrs981049067
dbSNP (classic)rs981049067
ClinGenrs981049067
ebirs981049067
HLIrs981049067
Exacrs981049067
Gnomadrs981049067
Varsomers981049067
LitVarrs981049067
Maprs981049067
PheGenIrs981049067
Biobankrs981049067
1000 genomesrs981049067
hgdprs981049067
ensemblrs981049067
geneviewrs981049067
scholarrs981049067
googlers981049067
pharmgkbrs981049067
gwascentralrs981049067
openSNPrs981049067
23andMers981049067
23andMe allrs981049067
SNPshotrs981049067
SNPdbers981049067
MSV3drs981049067
GWAS Ctlgrs981049067
Max Magnitude0
ClinVar
Risk rs981049067(A;A) rs981049067(C;C)
Alt rs981049067(A;A) rs981049067(C;C)
Reference Rs981049067(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 3
Variation info
Gene SDHC
CLNDBN Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 3
Reversed 0
HGVS NC_000001.10:g.161326612G>A; NC_000001.10:g.161326612G>C
CLNSRC
CLNACC RCV000492239.1, RCV000477028.1,