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rs796051948

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051948(A;G)
Make rs796051948(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107901804
GeneDLD
is asnp
is mentioned by
dbSNPrs796051948
ebirs796051948
HLIrs796051948
Exacrs796051948
Varsomers796051948
Maprs796051948
PheGenIrs796051948
hapmaprs796051948
1000 genomesrs796051948
hgdprs796051948
ensemblrs796051948
gopubmedrs796051948
geneviewrs796051948
scholarrs796051948
googlers796051948
pharmgkbrs796051948
gwascentralrs796051948
openSNPrs796051948
23andMers796051948
23andMe allrs796051948
SNP Nexus

SNPshotrs796051948
SNPdbers796051948
MSV3drs796051948
GWAS Ctlgrs796051948
Max Magnitude0
ClinVar
Risk rs796051948(G;G)
Alt rs796051948(G;G)
Reference rs796051948(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLD
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107542249A>G
CLNSRC
CLNACC RCV000185849.2,