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rs201286421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201286421(C;T)
Make rs201286421(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161323636
GeneSDHC
is asnp
is mentioned by
dbSNPrs201286421
ebirs201286421
HLIrs201286421
Exacrs201286421
Varsomers201286421
Maprs201286421
PheGenIrs201286421
hapmaprs201286421
1000 genomesrs201286421
hgdprs201286421
ensemblrs201286421
gopubmedrs201286421
geneviewrs201286421
scholarrs201286421
googlers201286421
pharmgkbrs201286421
gwascentralrs201286421
openSNPrs201286421
23andMers201286421
23andMe allrs201286421
SNP Nexus

SNPshotrs201286421
SNPdbers201286421
MSV3drs201286421
GWAS Ctlgrs201286421
Max Magnitude0
ClinVar
Risk rs201286421(T;T)
Alt rs201286421(T;T)
Reference rs201286421(C;C)
Significance Pathogenic
Disease Paragangliomas 3 Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor
Variation info
Gene SDHC
CLNDBN Paragangliomas 3 Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000001.10:g.161293426C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000034695.1, RCV000128874.2, RCV000231499.1,