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rs764611160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs764611160(-;-)
Make rs764611160(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107915624
GeneDLD
is asnp
is mentioned by
dbSNPrs764611160
dbSNP (classic)rs764611160
ClinGenrs764611160
ebirs764611160
HLIrs764611160
Exacrs764611160
Gnomadrs764611160
Varsomers764611160
LitVarrs764611160
Maprs764611160
PheGenIrs764611160
Biobankrs764611160
1000 genomesrs764611160
hgdprs764611160
ensemblrs764611160
geneviewrs764611160
scholarrs764611160
googlers764611160
pharmgkbrs764611160
gwascentralrs764611160
openSNPrs764611160
23andMers764611160
SNPshotrs764611160
SNPdbers764611160
MSV3drs764611160
GWAS Ctlgrs764611160
Max Magnitude0
ClinVar
Risk rs764611160(-;-)
Alt rs764611160(-;-)
Reference Rs764611160(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene DLD
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107556069_107556070delAG
CLNSRC
CLNACC RCV000482561.1,