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rs1064794269

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position17022627
GeneSDHB
is asnp
is mentioned by
dbSNPrs1064794269
dbSNP (old)rs1064794269
ClinGenrs1064794269
ebirs1064794269
HLIrs1064794269
Exacrs1064794269
Gnomadrs1064794269
Varsomers1064794269
Maprs1064794269
PheGenIrs1064794269
Biobankrs1064794269
1000 genomesrs1064794269
hgdprs1064794269
ensemblrs1064794269
gopubmedrs1064794269
geneviewrs1064794269
scholarrs1064794269
googlers1064794269
pharmgkbrs1064794269
gwascentralrs1064794269
openSNPrs1064794269
23andMers1064794269
23andMe allrs1064794269
SNPshotrs1064794269
SNPdbers1064794269
MSV3drs1064794269
GWAS Ctlgrs1064794269
Max Magnitude0
ClinVar
Risk rs1064794269(A;A)
Alt rs1064794269(A;A)
Reference Rs1064794269(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SDHB
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.17349122C>T
CLNSRC
CLNACC RCV000485327.1,