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rs886039690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039690(G;T)
Make rs886039690(T;T)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position19355685
GenePDHA1
is asnp
is mentioned by
dbSNPrs886039690
dbSNP (classic)rs886039690
ClinGenrs886039690
ebirs886039690
HLIrs886039690
Exacrs886039690
Gnomadrs886039690
Varsomers886039690
LitVarrs886039690
Maprs886039690
PheGenIrs886039690
Biobankrs886039690
1000 genomesrs886039690
hgdprs886039690
ensemblrs886039690
geneviewrs886039690
scholarrs886039690
googlers886039690
pharmgkbrs886039690
gwascentralrs886039690
openSNPrs886039690
23andMers886039690
23andMe allrs886039690
SNPshotrs886039690
SNPdbers886039690
MSV3drs886039690
GWAS Ctlgrs886039690
Max Magnitude0
ClinVar
Risk rs886039690(T;T)
Alt rs886039690(T;T)
Reference Rs886039690(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19373803G>T
CLNSRC
CLNACC RCV000255781.1,