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rs1060501226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501226(A;G)
Make rs1060501226(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position68738295
GeneCDH1
is asnp
is mentioned by
dbSNPrs1060501226
dbSNP (old)rs1060501226
ClinGenrs1060501226
ebirs1060501226
HLIrs1060501226
Exacrs1060501226
Gnomadrs1060501226
Varsomers1060501226
Maprs1060501226
PheGenIrs1060501226
Biobankrs1060501226
1000 genomesrs1060501226
hgdprs1060501226
ensemblrs1060501226
gopubmedrs1060501226
geneviewrs1060501226
scholarrs1060501226
googlers1060501226
pharmgkbrs1060501226
gwascentralrs1060501226
openSNPrs1060501226
23andMers1060501226
23andMe allrs1060501226
SNPshotrs1060501226
SNPdbers1060501226
MSV3drs1060501226
GWAS Ctlgrs1060501226
Max Magnitude0
ClinVar
Risk rs1060501226(G;G)
Alt rs1060501226(G;G)
Reference Rs1060501226(A;A)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68772198A>G
CLNSRC
CLNACC RCV000462976.1,