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rs794727621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794727621(C;C)
Make rs794727621(C;T)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position19351300
GenePDHA1
is asnp
is mentioned by
dbSNPrs794727621
dbSNP (classic)rs794727621
ClinGenrs794727621
ebirs794727621
HLIrs794727621
Exacrs794727621
Gnomadrs794727621
Varsomers794727621
LitVarrs794727621
Maprs794727621
PheGenIrs794727621
Biobankrs794727621
1000 genomesrs794727621
hgdprs794727621
ensemblrs794727621
geneviewrs794727621
scholarrs794727621
googlers794727621
pharmgkbrs794727621
gwascentralrs794727621
openSNPrs794727621
23andMers794727621
23andMe allrs794727621
SNPshotrs794727621
SNPdbers794727621
MSV3drs794727621
GWAS Ctlgrs794727621
Max Magnitude0
ClinVar
Risk rs794727621(C;C)
Alt rs794727621(C;C)
Reference Rs794727621(T;T)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene PDHA1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000023.10:g.19369418T>C
CLNSRC
CLNACC RCV000178069.3, RCV000259128.1,