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rs1060501244

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501244(A;A)
Make rs1060501244(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position68828204
GeneCDH1
is asnp
is mentioned by
dbSNPrs1060501244
dbSNP (old)rs1060501244
ClinGenrs1060501244
ebirs1060501244
HLIrs1060501244
Exacrs1060501244
Gnomadrs1060501244
Varsomers1060501244
Maprs1060501244
PheGenIrs1060501244
Biobankrs1060501244
1000 genomesrs1060501244
hgdprs1060501244
ensemblrs1060501244
gopubmedrs1060501244
geneviewrs1060501244
scholarrs1060501244
googlers1060501244
pharmgkbrs1060501244
gwascentralrs1060501244
openSNPrs1060501244
23andMers1060501244
23andMe allrs1060501244
SNPshotrs1060501244
SNPdbers1060501244
MSV3drs1060501244
GWAS Ctlgrs1060501244
Max Magnitude0
ClinVar
Risk rs1060501244(A;A)
Alt rs1060501244(A;A)
Reference Rs1060501244(G;G)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68862107G>A
CLNSRC
CLNACC RCV000475163.1, RCV000492116.1,