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rs1057517542

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517542(A;A)
Make rs1057517542(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position68829653
GeneCDH1
is asnp
is mentioned by
dbSNPrs1057517542
dbSNP (old)rs1057517542
ClinGenrs1057517542
ebirs1057517542
HLIrs1057517542
Exacrs1057517542
Gnomadrs1057517542
Varsomers1057517542
Maprs1057517542
PheGenIrs1057517542
Biobankrs1057517542
1000 genomesrs1057517542
hgdprs1057517542
ensemblrs1057517542
gopubmedrs1057517542
geneviewrs1057517542
scholarrs1057517542
googlers1057517542
pharmgkbrs1057517542
gwascentralrs1057517542
openSNPrs1057517542
23andMers1057517542
23andMe allrs1057517542
SNPshotrs1057517542
SNPdbers1057517542
MSV3drs1057517542
GWAS Ctlgrs1057517542
Max Magnitude0
ClinVar
Risk rs1057517542(A;A)
Alt rs1057517542(A;A)
Reference Rs1057517542(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.68863556G>A
CLNSRC
CLNACC RCV000410537.1, RCV000492413.1,