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rs727504457

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727504457(C;C)
Make rs727504457(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17033086
GeneSDHB
is asnp
is mentioned by
dbSNPrs727504457
ebirs727504457
HLIrs727504457
Exacrs727504457
Varsomers727504457
Maprs727504457
PheGenIrs727504457
hapmaprs727504457
1000 genomesrs727504457
hgdprs727504457
ensemblrs727504457
gopubmedrs727504457
geneviewrs727504457
scholarrs727504457
googlers727504457
pharmgkbrs727504457
gwascentralrs727504457
openSNPrs727504457
23andMers727504457
23andMe allrs727504457
SNP Nexus

SNPshotrs727504457
SNPdbers727504457
MSV3drs727504457
GWAS Ctlgrs727504457
Max Magnitude0
ClinVar
Risk rs727504457(C;C)
Alt rs727504457(C;C)
Reference rs727504457(T;T)
Significance Probable-Pathogenic
Disease Hereditary Paraganglioma-Pheochromocytoma Syndromes
Variation info
Gene SDHB
CLNDBN Hereditary Paraganglioma-Pheochromocytoma Syndromes
Reversed 1
HGVS NC_000001.10:g.17359581A>G
CLNSRC
CLNACC RCV000155443.1,