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rs786205456

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205456(A;A)
Make rs786205456(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position14935524
GeneDCLRE1C
is asnp
is mentioned by
dbSNPrs786205456
ebirs786205456
HLIrs786205456
Exacrs786205456
Varsomers786205456
Maprs786205456
PheGenIrs786205456
hapmaprs786205456
1000 genomesrs786205456
hgdprs786205456
ensemblrs786205456
gopubmedrs786205456
geneviewrs786205456
scholarrs786205456
googlers786205456
pharmgkbrs786205456
gwascentralrs786205456
openSNPrs786205456
23andMers786205456
23andMe allrs786205456
SNP Nexus

SNPshotrs786205456
SNPdbers786205456
MSV3drs786205456
GWAS Ctlgrs786205456
Max Magnitude0
ClinVar
Risk rs786205456(A;A)
Alt rs786205456(A;A)
Reference rs786205456(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DCLRE1C
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.14977523C>T
CLNSRC
CLNACC RCV000171174.1,