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rs863224209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0 common genotype
Make rs863224209(-;-)
Make rs863224209(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position185145175
GeneSLC25A4
is asnp
is mentioned by
dbSNPrs863224209
dbSNP (classic)rs863224209
ClinGenrs863224209
ebirs863224209
HLIrs863224209
Exacrs863224209
Gnomadrs863224209
Varsomers863224209
LitVarrs863224209
Maprs863224209
PheGenIrs863224209
Biobankrs863224209
1000 genomesrs863224209
hgdprs863224209
ensemblrs863224209
geneviewrs863224209
scholarrs863224209
googlers863224209
pharmgkbrs863224209
gwascentralrs863224209
openSNPrs863224209
23andMers863224209
SNPshotrs863224209
SNPdbers863224209
MSV3drs863224209
GWAS Ctlgrs863224209
Max Magnitude0
ClinVar
Risk rs863224209(-;-)
Alt rs863224209(-;-)
Reference Rs863224209(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC25A4
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.186066329delC
CLNSRC
CLNACC RCV000196453.1,