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rs745949756

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs745949756(A;G)
Make rs745949756(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position34994922
GenePDHX
is asnp
is mentioned by
dbSNPrs745949756
ebirs745949756
HLIrs745949756
Exacrs745949756
Varsomers745949756
Maprs745949756
PheGenIrs745949756
hapmaprs745949756
1000 genomesrs745949756
hgdprs745949756
ensemblrs745949756
gopubmedrs745949756
geneviewrs745949756
scholarrs745949756
googlers745949756
pharmgkbrs745949756
gwascentralrs745949756
openSNPrs745949756
23andMers745949756
23andMe allrs745949756
SNP Nexus

SNPshotrs745949756
SNPdbers745949756
MSV3drs745949756
GWAS Ctlgrs745949756
Max Magnitude0
ClinVar
Risk rs745949756(G;G)
Alt rs745949756(G;G)
Reference rs745949756(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDHX
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.35016469A>G
CLNSRC
CLNACC RCV000197652.2,