Rs116093741

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs116093741(A;G)
Make rs116093741(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position68812144
GeneCDH1
is asnp
is mentioned by
dbSNPrs116093741
Exacrs116093741
PheGenIrs116093741
nextbiors116093741
hapmaprs116093741
1000 genomesrs116093741
hgdprs116093741
ensemblrs116093741
gopubmedrs116093741
geneviewrs116093741
scholarrs116093741
googlers116093741
pharmgkbrs116093741
gwascentralrs116093741
openSNPrs116093741
23andMers116093741
23andMe allrs116093741
SNP Nexus

SNPshotrs116093741
SNPdbers116093741
MSV3drs116093741
GMAF0.0004591
Max Magnitude0
OMIM192090
Desc
Variant0016
Relatedalso
ClinVar
Risk rs116093741(G;G)
Alt rs116093741(G;G)
Reference rs116093741(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.68846047A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013032.23,