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rs886037822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886037822(-;-)
Make rs886037822(-;C)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position68813395
GeneCDH1
is asnp
is mentioned by
dbSNPrs886037822
dbSNP (classic)rs886037822
ClinGenrs886037822
ebirs886037822
HLIrs886037822
Exacrs886037822
Gnomadrs886037822
Varsomers886037822
LitVarrs886037822
Maprs886037822
PheGenIrs886037822
Biobankrs886037822
1000 genomesrs886037822
hgdprs886037822
ensemblrs886037822
geneviewrs886037822
scholarrs886037822
googlers886037822
pharmgkbrs886037822
gwascentralrs886037822
openSNPrs886037822
23andMers886037822
SNPshotrs886037822
SNPdbers886037822
MSV3drs886037822
GWAS Ctlgrs886037822
Max Magnitude0
ClinVar
Risk rs886037822(-;-)
Alt rs886037822(-;-)
Reference Rs886037822(C;C)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68847298delC
CLNSRC
CLNACC RCV000240878.1,