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rs570278423

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs570278423(C;T)
Make rs570278423(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17033077
GeneSDHB
is asnp
is mentioned by
dbSNPrs570278423
ebirs570278423
HLIrs570278423
Exacrs570278423
Varsomers570278423
Maprs570278423
PheGenIrs570278423
hapmaprs570278423
1000 genomesrs570278423
hgdprs570278423
ensemblrs570278423
gopubmedrs570278423
geneviewrs570278423
scholarrs570278423
googlers570278423
pharmgkbrs570278423
gwascentralrs570278423
openSNPrs570278423
23andMers570278423
23andMe allrs570278423
SNP Nexus

SNPshotrs570278423
SNPdbers570278423
MSV3drs570278423
GWAS Ctlgrs570278423
Max Magnitude0
ClinVar
Risk rs570278423(T;T)
Alt rs570278423(T;T)
Reference rs570278423(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SDHB
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.17359572C>T
CLNSRC
CLNACC RCV000183223.1,