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rs796051949

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051949(A;C)
Make rs796051949(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107902343
GeneDLD
is asnp
is mentioned by
dbSNPrs796051949
ebirs796051949
HLIrs796051949
Exacrs796051949
Varsomers796051949
Maprs796051949
PheGenIrs796051949
hapmaprs796051949
1000 genomesrs796051949
hgdprs796051949
ensemblrs796051949
gopubmedrs796051949
geneviewrs796051949
scholarrs796051949
googlers796051949
pharmgkbrs796051949
gwascentralrs796051949
openSNPrs796051949
23andMers796051949
23andMe allrs796051949
SNP Nexus

SNPshotrs796051949
SNPdbers796051949
MSV3drs796051949
GWAS Ctlgrs796051949
Max Magnitude0
ClinVar
Risk rs796051949(C;C)
Alt rs796051949(C;C)
Reference rs796051949(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLD
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107542788A>C
CLNSRC
CLNACC RCV000185850.1,