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rs771317809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771317809(C;T)
Make rs771317809(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position50470140
GeneDDC
is asnp
is mentioned by
dbSNPrs771317809
dbSNP (classic)rs771317809
ClinGenrs771317809
ebirs771317809
HLIrs771317809
Exacrs771317809
Gnomadrs771317809
Varsomers771317809
LitVarrs771317809
Maprs771317809
PheGenIrs771317809
Biobankrs771317809
1000 genomesrs771317809
hgdprs771317809
ensemblrs771317809
geneviewrs771317809
scholarrs771317809
googlers771317809
pharmgkbrs771317809
gwascentralrs771317809
openSNPrs771317809
23andMers771317809
23andMe allrs771317809
SNPshotrs771317809
SNPdbers771317809
MSV3drs771317809
GWAS Ctlgrs771317809
Max Magnitude0
ClinVar
Risk rs771317809(T;T)
Alt rs771317809(T;T)
Reference Rs771317809(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DDC
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.50537838C>T
CLNSRC
CLNACC RCV000445005.1,