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rs786205489

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205489(C;C)
Make rs786205489(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position91291030
GeneCCDC88C
is asnp
is mentioned by
dbSNPrs786205489
ebirs786205489
HLIrs786205489
Exacrs786205489
Varsomers786205489
Maprs786205489
PheGenIrs786205489
hapmaprs786205489
1000 genomesrs786205489
hgdprs786205489
ensemblrs786205489
gopubmedrs786205489
geneviewrs786205489
scholarrs786205489
googlers786205489
pharmgkbrs786205489
gwascentralrs786205489
openSNPrs786205489
23andMers786205489
23andMe allrs786205489
SNP Nexus

SNPshotrs786205489
SNPdbers786205489
MSV3drs786205489
GWAS Ctlgrs786205489
Max Magnitude0
ClinVar
Risk rs786205489(C;C)
Alt rs786205489(C;C)
Reference rs786205489(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CCDC88C
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.91757374C>G
CLNSRC
CLNACC RCV000171227.1,