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rs387906780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906780(C;T)
Make rs387906780(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position251439
GeneSDHA
is asnp
is mentioned by
dbSNPrs387906780
ebirs387906780
HLIrs387906780
Exacrs387906780
Varsomers387906780
Maprs387906780
PheGenIrs387906780
hapmaprs387906780
1000 genomesrs387906780
hgdprs387906780
ensemblrs387906780
gopubmedrs387906780
geneviewrs387906780
scholarrs387906780
googlers387906780
pharmgkbrs387906780
gwascentralrs387906780
openSNPrs387906780
23andMers387906780
23andMe allrs387906780
SNP Nexus

SNPshotrs387906780
SNPdbers387906780
MSV3drs387906780
GWAS Ctlgrs387906780
Max Magnitude0
ClinVar
Risk rs387906780(T;T)
Alt rs387906780(T;T)
Reference rs387906780(C;C)
Significance Pathogenic
Disease Paragangliomas 5
Variation info
Gene SDHA
CLNDBN Paragangliomas 5
Reversed 0
HGVS NC_000005.9:g.251554C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023042.4,