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rs796053242

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs796053242(-;-)
Make rs796053242(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position792310
GeneSLC25A22
is asnp
is mentioned by
dbSNPrs796053242
dbSNP (old)rs796053242
ClinGenrs796053242
ebirs796053242
HLIrs796053242
Exacrs796053242
Gnomadrs796053242
Varsomers796053242
Maprs796053242
PheGenIrs796053242
Biobankrs796053242
1000 genomesrs796053242
hgdprs796053242
ensemblrs796053242
gopubmedrs796053242
geneviewrs796053242
scholarrs796053242
googlers796053242
pharmgkbrs796053242
gwascentralrs796053242
openSNPrs796053242
23andMers796053242
23andMe allrs796053242
SNP Nexus

SNPshotrs796053242
SNPdbers796053242
MSV3drs796053242
GWAS Ctlgrs796053242
Max Magnitude0
ClinVar
Risk rs796053242(-;-)
Alt rs796053242(-;-)
Reference Rs796053242(CT;CT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC25A22
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.792310_792311delAG
CLNSRC
CLNACC RCV000189333.2,