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rs763303046

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs763303046(A;T)
Make rs763303046(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107901780
GeneDLD
is asnp
is mentioned by
dbSNPrs763303046
dbSNP (classic)rs763303046
ClinGenrs763303046
ebirs763303046
HLIrs763303046
Exacrs763303046
Gnomadrs763303046
Varsomers763303046
LitVarrs763303046
Maprs763303046
PheGenIrs763303046
Biobankrs763303046
1000 genomesrs763303046
hgdprs763303046
ensemblrs763303046
geneviewrs763303046
scholarrs763303046
googlers763303046
pharmgkbrs763303046
gwascentralrs763303046
openSNPrs763303046
23andMers763303046
SNPshotrs763303046
SNPdbers763303046
MSV3drs763303046
GWAS Ctlgrs763303046
Max Magnitude0
ClinVar
Risk rs763303046(G;G) rs763303046(T;T)
Alt rs763303046(G;G) rs763303046(T;T)
Reference Rs763303046(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLD
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107542225A>G
CLNSRC
CLNACC RCV000484591.1,