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rs786203727

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203727(G;T)
Make rs786203727(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68801691
GeneCDH1
is asnp
is mentioned by
dbSNPrs786203727
ebirs786203727
HLIrs786203727
Exacrs786203727
Varsomers786203727
Maprs786203727
PheGenIrs786203727
hapmaprs786203727
1000 genomesrs786203727
hgdprs786203727
ensemblrs786203727
gopubmedrs786203727
geneviewrs786203727
scholarrs786203727
googlers786203727
pharmgkbrs786203727
gwascentralrs786203727
openSNPrs786203727
23andMers786203727
23andMe allrs786203727
SNP Nexus

SNPshotrs786203727
SNPdbers786203727
MSV3drs786203727
GWAS Ctlgrs786203727
Max Magnitude0
ClinVar
Risk rs786203727(T;T)
Alt rs786203727(T;T)
Reference rs786203727(G;G)
Significance Unknown
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68835594G>T
CLNSRC
CLNACC RCV000167156.1,