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rs794728950

From SNPedia

Orientationminus
Geno Mag Summary
(CTAT;CTAT) 0 common in clinvar
Make rs794728950(-;-)
Make rs794728950(-;CTAT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17022652
GeneSDHB
is asnp
is mentioned by
dbSNPrs794728950
ebirs794728950
HLIrs794728950
Exacrs794728950
Varsomers794728950
Maprs794728950
PheGenIrs794728950
hapmaprs794728950
1000 genomesrs794728950
hgdprs794728950
ensemblrs794728950
gopubmedrs794728950
geneviewrs794728950
scholarrs794728950
googlers794728950
pharmgkbrs794728950
gwascentralrs794728950
openSNPrs794728950
23andMers794728950
23andMe allrs794728950
SNP Nexus

SNPshotrs794728950
SNPdbers794728950
MSV3drs794728950
GWAS Ctlgrs794728950
Max Magnitude0
ClinVar
Risk rs794728950(;)
Alt rs794728950(;)
Reference rs794728950(CTAT;CTAT)
Significance Pathogenic
Disease not provided
Variation info
Gene SDHB
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.17349147_17349150delATAG
CLNSRC
CLNACC RCV000183221.1,