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rs794728946

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728946(G;T)
Make rs794728946(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17027763
GeneSDHB
is asnp
is mentioned by
dbSNPrs794728946
ebirs794728946
HLIrs794728946
Exacrs794728946
Varsomers794728946
Maprs794728946
PheGenIrs794728946
hapmaprs794728946
1000 genomesrs794728946
hgdprs794728946
ensemblrs794728946
gopubmedrs794728946
geneviewrs794728946
scholarrs794728946
googlers794728946
pharmgkbrs794728946
gwascentralrs794728946
openSNPrs794728946
23andMers794728946
23andMe allrs794728946
SNP Nexus

SNPshotrs794728946
SNPdbers794728946
MSV3drs794728946
GWAS Ctlgrs794728946
Max Magnitude0
ClinVar
Risk rs794728946(T;T)
Alt rs794728946(T;T)
Reference rs794728946(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SDHB
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.17354258C>A
CLNSRC
CLNACC RCV000183214.1,