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rs199959402

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199959402(C;T)
Make rs199959402(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19351368
GenePDHA1
is asnp
is mentioned by
dbSNPrs199959402
ebirs199959402
HLIrs199959402
Exacrs199959402
Varsomers199959402
Maprs199959402
PheGenIrs199959402
hapmaprs199959402
1000 genomesrs199959402
hgdprs199959402
ensemblrs199959402
gopubmedrs199959402
geneviewrs199959402
scholarrs199959402
googlers199959402
pharmgkbrs199959402
gwascentralrs199959402
openSNPrs199959402
23andMers199959402
23andMe allrs199959402
SNP Nexus

SNPshotrs199959402
SNPdbers199959402
MSV3drs199959402
GWAS Ctlgrs199959402
Max Magnitude0
ClinVar
Risk rs199959402(T;T)
Alt rs199959402(T;T)
Reference rs199959402(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19369486C>T
CLNSRC
CLNACC RCV000196836.1,