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rs747810875

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747810875(C;T)
Make rs747810875(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107893265
GeneDLD
is asnp
is mentioned by
dbSNPrs747810875
dbSNP (classic)rs747810875
ClinGenrs747810875
ebirs747810875
HLIrs747810875
Exacrs747810875
Gnomadrs747810875
Varsomers747810875
LitVarrs747810875
Maprs747810875
PheGenIrs747810875
Biobankrs747810875
1000 genomesrs747810875
hgdprs747810875
ensemblrs747810875
geneviewrs747810875
scholarrs747810875
googlers747810875
pharmgkbrs747810875
gwascentralrs747810875
openSNPrs747810875
23andMers747810875
SNPshotrs747810875
SNPdbers747810875
MSV3drs747810875
GWAS Ctlgrs747810875
Max Magnitude0
ClinVar
Risk rs747810875(G;G) rs747810875(T;T)
Alt rs747810875(G;G) rs747810875(T;T)
Reference Rs747810875(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene DLD
CLNDBN not provided not specified
Reversed 0
HGVS NC_000007.13:g.107533710C>G; NC_000007.13:g.107533710C>T
CLNSRC
CLNACC RCV000479643.1, RCV000252044.1,