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rs796051947

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051947(C;T)
Make rs796051947(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107901801
GeneDLD
is asnp
is mentioned by
dbSNPrs796051947
ebirs796051947
HLIrs796051947
Exacrs796051947
Varsomers796051947
Maprs796051947
PheGenIrs796051947
hapmaprs796051947
1000 genomesrs796051947
hgdprs796051947
ensemblrs796051947
gopubmedrs796051947
geneviewrs796051947
scholarrs796051947
googlers796051947
pharmgkbrs796051947
gwascentralrs796051947
openSNPrs796051947
23andMers796051947
23andMe allrs796051947
SNP Nexus

SNPshotrs796051947
SNPdbers796051947
MSV3drs796051947
GWAS Ctlgrs796051947
Max Magnitude0
ClinVar
Risk rs796051947(T;T)
Alt rs796051947(T;T)
Reference rs796051947(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLD
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107542246C>T
CLNSRC
CLNACC RCV000185848.1,