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rs1057518180

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518180(-;A)
Make rs1057518180(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position34966791
GenePDHX
is asnp
is mentioned by
dbSNPrs1057518180
dbSNP (old)rs1057518180
ClinGenrs1057518180
ebirs1057518180
HLIrs1057518180
Exacrs1057518180
Gnomadrs1057518180
Varsomers1057518180
LitVarrs1057518180
Maprs1057518180
PheGenIrs1057518180
Biobankrs1057518180
1000 genomesrs1057518180
hgdprs1057518180
ensemblrs1057518180
gopubmedrs1057518180
geneviewrs1057518180
scholarrs1057518180
googlers1057518180
pharmgkbrs1057518180
gwascentralrs1057518180
openSNPrs1057518180
23andMers1057518180
23andMe allrs1057518180
SNPshotrs1057518180
SNPdbers1057518180
MSV3drs1057518180
GWAS Ctlgrs1057518180
Max Magnitude0
ClinVar
Risk rs1057518180(A;A)
Alt rs1057518180(A;A)
Reference Rs1057518180(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHX
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.34988338dupA
CLNSRC
CLNACC RCV000413565.1,