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rs786205568

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205568(A;A)
Make rs786205568(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15596208
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs786205568
ebirs786205568
HLIrs786205568
Exacrs786205568
Varsomers786205568
Maprs786205568
PheGenIrs786205568
hapmaprs786205568
1000 genomesrs786205568
hgdprs786205568
ensemblrs786205568
gopubmedrs786205568
geneviewrs786205568
scholarrs786205568
googlers786205568
pharmgkbrs786205568
gwascentralrs786205568
openSNPrs786205568
23andMers786205568
23andMe allrs786205568
SNP Nexus

SNPshotrs786205568
SNPdbers786205568
MSV3drs786205568
GWAS Ctlgrs786205568
Max Magnitude0
ClinVar
Risk rs786205568(A;A)
Alt rs786205568(A;A)
Reference rs786205568(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CC2D2A
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.15597831G>A
CLNSRC
CLNACC RCV000171374.1,