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rs33935154

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs33935154(A;A)
Make rs33935154(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position68822138
GeneCDH1
is asnp
is mentioned by
dbSNPrs33935154
ebirs33935154
HLIrs33935154
Exacrs33935154
Varsomers33935154
Maprs33935154
PheGenIrs33935154
hapmaprs33935154
1000 genomesrs33935154
hgdprs33935154
ensemblrs33935154
gopubmedrs33935154
geneviewrs33935154
scholarrs33935154
googlers33935154
pharmgkbrs33935154
gwascentralrs33935154
openSNPrs33935154
23andMers33935154
23andMe allrs33935154
SNP Nexus

SNPshotrs33935154
SNPdbers33935154
MSV3drs33935154
GWAS Ctlgrs33935154
GMAF0.0101
Max Magnitude0
OMIM192090
Desc
Variant0002
Relatedalso


ClinVar
Risk rs33935154(A;A)
Alt rs33935154(A;A)
Reference rs33935154(G;G)
Significance Other
Disease Endometrial carcinoma Hereditary diffuse gastric cancer not provided not specified Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Endometrial carcinoma Hereditary diffuse gastric cancer not provided not specified Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68856041G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013018.4, RCV000013019.24, RCV000034706.3, RCV000120500.2, RCV000130292.4,