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rs1060501237

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501237(C;C)
Make rs1060501237(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position68811861
GeneCDH1
is asnp
is mentioned by
dbSNPrs1060501237
dbSNP (old)rs1060501237
ClinGenrs1060501237
ebirs1060501237
HLIrs1060501237
Exacrs1060501237
Gnomadrs1060501237
Varsomers1060501237
Maprs1060501237
PheGenIrs1060501237
Biobankrs1060501237
1000 genomesrs1060501237
hgdprs1060501237
ensemblrs1060501237
gopubmedrs1060501237
geneviewrs1060501237
scholarrs1060501237
googlers1060501237
pharmgkbrs1060501237
gwascentralrs1060501237
openSNPrs1060501237
23andMers1060501237
23andMe allrs1060501237
SNPshotrs1060501237
SNPdbers1060501237
MSV3drs1060501237
GWAS Ctlgrs1060501237
Max Magnitude0
ClinVar
Risk rs1060501237(C;C)
Alt rs1060501237(C;C)
Reference Rs1060501237(T;T)
Significance Probable-Pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68845764T>C
CLNSRC
CLNACC RCV000461959.1,