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rs863224234

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224234(C;T)
Make rs863224234(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101348565
GeneTIMM8A
is asnp
is mentioned by
dbSNPrs863224234
ebirs863224234
HLIrs863224234
Exacrs863224234
Varsomers863224234
Maprs863224234
PheGenIrs863224234
hapmaprs863224234
1000 genomesrs863224234
hgdprs863224234
ensemblrs863224234
gopubmedrs863224234
geneviewrs863224234
scholarrs863224234
googlers863224234
pharmgkbrs863224234
gwascentralrs863224234
openSNPrs863224234
23andMers863224234
23andMe allrs863224234
SNP Nexus

SNPshotrs863224234
SNPdbers863224234
MSV3drs863224234
GWAS Ctlgrs863224234
Max Magnitude0
ClinVar
Risk rs863224234(T;T)
Alt rs863224234(T;T)
Reference rs863224234(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TIMM8A
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100603553G>A
CLNSRC
CLNACC RCV000197115.1,