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rs202166915

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202166915(A;A)
Make rs202166915(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19355710
GenePDHA1
is asnp
is mentioned by
dbSNPrs202166915
ebirs202166915
HLIrs202166915
Exacrs202166915
Varsomers202166915
Maprs202166915
PheGenIrs202166915
hapmaprs202166915
1000 genomesrs202166915
hgdprs202166915
ensemblrs202166915
gopubmedrs202166915
geneviewrs202166915
scholarrs202166915
googlers202166915
pharmgkbrs202166915
gwascentralrs202166915
openSNPrs202166915
23andMers202166915
23andMe allrs202166915
SNP Nexus

SNPshotrs202166915
SNPdbers202166915
MSV3drs202166915
GWAS Ctlgrs202166915
Max Magnitude0
ClinVar
Risk rs202166915(A;A)
Alt rs202166915(A;A)
Reference rs202166915(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases not specified
Variation info
Gene PDHA1
CLNDBN Inborn genetic diseases not specified
Reversed 0
HGVS NC_000023.10:g.19373828G>A
CLNSRC
CLNACC RCV000190809.1, RCV000200145.1,