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rs200397144

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200397144(C;T)
Make rs200397144(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position251427
GeneSDHA
is asnp
is mentioned by
dbSNPrs200397144
ebirs200397144
HLIrs200397144
Exacrs200397144
Varsomers200397144
Maprs200397144
PheGenIrs200397144
hapmaprs200397144
1000 genomesrs200397144
hgdprs200397144
ensemblrs200397144
gopubmedrs200397144
geneviewrs200397144
scholarrs200397144
googlers200397144
pharmgkbrs200397144
gwascentralrs200397144
openSNPrs200397144
23andMers200397144
23andMe allrs200397144
SNP Nexus

SNPshotrs200397144
SNPdbers200397144
MSV3drs200397144
GWAS Ctlgrs200397144
Max Magnitude0
ClinVar
Risk rs200397144(T;T)
Alt rs200397144(T;T)
Reference rs200397144(C;C)
Significance Pathogenic
Disease Paragangliomas 5 Hereditary cancer-predisposing syndrome
Variation info
Gene SDHA
CLNDBN Paragangliomas 5 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.251542C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000148027.1, RCV000163558.1,