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rs796053238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs796053238(-;-)
Make rs796053238(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position794773
GeneSLC25A22
is asnp
is mentioned by
dbSNPrs796053238
ClinGenrs796053238
ebirs796053238
HLIrs796053238
Exacrs796053238
Varsomers796053238
Maprs796053238
PheGenIrs796053238
hapmaprs796053238
1000 genomesrs796053238
hgdprs796053238
ensemblrs796053238
gopubmedrs796053238
geneviewrs796053238
scholarrs796053238
googlers796053238
pharmgkbrs796053238
gwascentralrs796053238
openSNPrs796053238
23andMers796053238
23andMe allrs796053238
SNP Nexus

SNPshotrs796053238
SNPdbers796053238
MSV3drs796053238
GWAS Ctlgrs796053238
Max Magnitude0
ClinVar
Risk rs796053238(-;-)
Alt rs796053238(-;-)
Reference Rs796053238(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC25A22
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.794773_794774delCA
CLNSRC
CLNACC RCV000189322.1,