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rs763399323

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763399323(C;T)
Make rs763399323(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position84200638
GeneCDHR1
is asnp
is mentioned by
dbSNPrs763399323
ebirs763399323
HLIrs763399323
Exacrs763399323
Varsomers763399323
Maprs763399323
PheGenIrs763399323
hapmaprs763399323
1000 genomesrs763399323
hgdprs763399323
ensemblrs763399323
gopubmedrs763399323
geneviewrs763399323
scholarrs763399323
googlers763399323
pharmgkbrs763399323
gwascentralrs763399323
openSNPrs763399323
23andMers763399323
23andMe allrs763399323
SNP Nexus

SNPshotrs763399323
SNPdbers763399323
MSV3drs763399323
GWAS Ctlgrs763399323
Max Magnitude0
ClinVar
Risk rs763399323(T;T)
Alt rs763399323(T;T)
Reference rs763399323(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDHR1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.85960394C>A
CLNSRC
CLNACC RCV000171179.1,