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rs757275923

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757275923(A;A)
Make rs757275923(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position107919017
GeneDLD
is asnp
is mentioned by
dbSNPrs757275923
ebirs757275923
HLIrs757275923
Exacrs757275923
Varsomers757275923
Maprs757275923
PheGenIrs757275923
hapmaprs757275923
1000 genomesrs757275923
hgdprs757275923
ensemblrs757275923
gopubmedrs757275923
geneviewrs757275923
scholarrs757275923
googlers757275923
pharmgkbrs757275923
gwascentralrs757275923
openSNPrs757275923
23andMers757275923
23andMe allrs757275923
SNP Nexus

SNPshotrs757275923
SNPdbers757275923
MSV3drs757275923
GWAS Ctlgrs757275923
Max Magnitude0
ClinVar
Risk rs757275923(A;A)
Alt rs757275923(A;A)
Reference rs757275923(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLD
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107559462G>A
CLNSRC
CLNACC RCV000185861.1,