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rs137854570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854570(C;G)
Make rs137854570(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position112837732
GeneAPC
is asnp
is mentioned by
dbSNPrs137854570
ebirs137854570
HLIrs137854570
Exacrs137854570
Varsomers137854570
Maprs137854570
PheGenIrs137854570
hapmaprs137854570
1000 genomesrs137854570
hgdprs137854570
ensemblrs137854570
gopubmedrs137854570
geneviewrs137854570
scholarrs137854570
googlers137854570
pharmgkbrs137854570
gwascentralrs137854570
openSNPrs137854570
23andMers137854570
23andMe allrs137854570
SNP Nexus

SNPshotrs137854570
SNPdbers137854570
MSV3drs137854570
GWAS Ctlgrs137854570
Max Magnitude0
OMIM611731
Desc
Variant0008
Relatedalso
ClinVar
Risk rs137854570(G;G)
Alt rs137854570(G;G)
Reference rs137854570(C;C)
Significance Pathogenic
Disease Gardner syndrome
Variation info
Gene APC
CLNDBN Gardner syndrome
Reversed 0
HGVS NC_000005.9:g.112173429C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000837.4,