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rs786205459

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205459(A;A)
Make rs786205459(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position84211698
GeneCDHR1
is asnp
is mentioned by
dbSNPrs786205459
ebirs786205459
HLIrs786205459
Exacrs786205459
Varsomers786205459
Maprs786205459
PheGenIrs786205459
hapmaprs786205459
1000 genomesrs786205459
hgdprs786205459
ensemblrs786205459
gopubmedrs786205459
geneviewrs786205459
scholarrs786205459
googlers786205459
pharmgkbrs786205459
gwascentralrs786205459
openSNPrs786205459
23andMers786205459
23andMe allrs786205459
SNP Nexus

SNPshotrs786205459
SNPdbers786205459
MSV3drs786205459
GWAS Ctlgrs786205459
Max Magnitude0
ClinVar
Risk rs786205459(A;A)
Alt rs786205459(A;A)
Reference rs786205459(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDHR1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.85971454T>A
CLNSRC
CLNACC RCV000171180.1,