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rs28933379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28933379(A;A)
Make rs28933379(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position112838953
GeneAPC
is asnp
is mentioned by
dbSNPrs28933379
ebirs28933379
HLIrs28933379
Exacrs28933379
Varsomers28933379
Maprs28933379
PheGenIrs28933379
hapmaprs28933379
1000 genomesrs28933379
hgdprs28933379
ensemblrs28933379
gopubmedrs28933379
geneviewrs28933379
scholarrs28933379
googlers28933379
pharmgkbrs28933379
gwascentralrs28933379
openSNPrs28933379
23andMers28933379
23andMe allrs28933379
SNP Nexus

SNPshotrs28933379
SNPdbers28933379
MSV3drs28933379
GWAS Ctlgrs28933379
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM175100
DescGASTRIC CANCER, SOMATIC
Variant0010
Relatedalso
Neighborrs1801155
Distance561
Neighborrs28933380
Distance560
OMIM611731
Desc
Variant0010
Relatedalso


ClinVar
Risk rs28933379(A;A)
Alt rs28933379(A;A)
Reference rs28933379(G;G)
Significance Pathogenic
Disease Neoplasm of stomach
Variation info
Gene APC
CLNDBN Neoplasm of stomach
Reversed 0
HGVS NC_000005.9:g.112174650G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000839.4,