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rs786205613

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205613(-;-)
Make rs786205613(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position84203048
GeneCDHR1
is asnp
is mentioned by
dbSNPrs786205613
ebirs786205613
HLIrs786205613
Exacrs786205613
Varsomers786205613
Maprs786205613
PheGenIrs786205613
hapmaprs786205613
1000 genomesrs786205613
hgdprs786205613
ensemblrs786205613
gopubmedrs786205613
geneviewrs786205613
scholarrs786205613
googlers786205613
pharmgkbrs786205613
gwascentralrs786205613
openSNPrs786205613
23andMers786205613
23andMe allrs786205613
SNP Nexus

SNPshotrs786205613
SNPdbers786205613
MSV3drs786205613
GWAS Ctlgrs786205613
Max Magnitude0
ClinVar
Risk rs786205613(;)
Alt rs786205613(;)
Reference rs786205613(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDHR1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.85962804delG
CLNSRC
CLNACC RCV000171458.1,