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rs797044957

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044957(G;G)
Make rs797044957(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position112028603
GeneDLAT
is asnp
is mentioned by
dbSNPrs797044957
ebirs797044957
HLIrs797044957
Exacrs797044957
Varsomers797044957
Maprs797044957
PheGenIrs797044957
hapmaprs797044957
1000 genomesrs797044957
hgdprs797044957
ensemblrs797044957
gopubmedrs797044957
geneviewrs797044957
scholarrs797044957
googlers797044957
pharmgkbrs797044957
gwascentralrs797044957
openSNPrs797044957
23andMers797044957
23andMe allrs797044957
SNP Nexus

SNPshotrs797044957
SNPdbers797044957
MSV3drs797044957
GWAS Ctlgrs797044957
Max Magnitude0
ClinVar
Risk rs797044957(G;G)
Alt rs797044957(G;G)
Reference rs797044957(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DLAT
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.111899327T>G
CLNSRC
CLNACC RCV000190817.1,