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rs863224147

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224147(C;T)
Make rs863224147(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19359612
GeneMAP3K15, PDHA1
is asnp
is mentioned by
dbSNPrs863224147
ebirs863224147
HLIrs863224147
Exacrs863224147
Varsomers863224147
Maprs863224147
PheGenIrs863224147
hapmaprs863224147
1000 genomesrs863224147
hgdprs863224147
ensemblrs863224147
gopubmedrs863224147
geneviewrs863224147
scholarrs863224147
googlers863224147
pharmgkbrs863224147
gwascentralrs863224147
openSNPrs863224147
23andMers863224147
23andMe allrs863224147
SNP Nexus

SNPshotrs863224147
SNPdbers863224147
MSV3drs863224147
GWAS Ctlgrs863224147
Max Magnitude0
ClinVar
Risk rs863224147(T;T)
Alt rs863224147(T;T)
Reference rs863224147(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1 MAP3K15
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19377730C>T
CLNSRC
CLNACC RCV000198575.1,