Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064794270

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position17028738
GeneSDHB
is asnp
is mentioned by
dbSNPrs1064794270
dbSNP (old)rs1064794270
ClinGenrs1064794270
ebirs1064794270
HLIrs1064794270
Exacrs1064794270
Gnomadrs1064794270
Varsomers1064794270
LitVarrs1064794270
Maprs1064794270
PheGenIrs1064794270
Biobankrs1064794270
1000 genomesrs1064794270
hgdprs1064794270
ensemblrs1064794270
gopubmedrs1064794270
geneviewrs1064794270
scholarrs1064794270
googlers1064794270
pharmgkbrs1064794270
gwascentralrs1064794270
openSNPrs1064794270
23andMers1064794270
23andMe allrs1064794270
SNPshotrs1064794270
SNPdbers1064794270
MSV3drs1064794270
GWAS Ctlgrs1064794270
Max Magnitude0
ClinVar
Risk rs1064794270(G;G)
Alt rs1064794270(G;G)
Reference Rs1064794270(A;A)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17355233T>C
CLNSRC
CLNACC RCV000486186.1, RCV000492665.1,