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rs863224156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224156(-;AAGT)
Make rs863224156(AAGT;AAGT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19359642
GeneMAP3K15, PDHA1
is asnp
is mentioned by
dbSNPrs863224156
dbSNP (classic)rs863224156
ClinGenrs863224156
ebirs863224156
HLIrs863224156
Exacrs863224156
Gnomadrs863224156
Varsomers863224156
LitVarrs863224156
Maprs863224156
PheGenIrs863224156
Biobankrs863224156
1000 genomesrs863224156
hgdprs863224156
ensemblrs863224156
geneviewrs863224156
scholarrs863224156
googlers863224156
pharmgkbrs863224156
gwascentralrs863224156
openSNPrs863224156
23andMers863224156
SNPshotrs863224156
SNPdbers863224156
MSV3drs863224156
GWAS Ctlgrs863224156
Max Magnitude0
ClinVar
Risk rs863224156(TAAG;TAAG)
Alt rs863224156(TAAG;TAAG)
Reference Rs863224156(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1 MAP3K15
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19377757_19377760dupAAGT
CLNSRC
CLNACC RCV000195575.1,