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rs1057518472

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518472(G;T)
Make rs1057518472(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112839201
GeneAPC
is asnp
is mentioned by
dbSNPrs1057518472
dbSNP (old)rs1057518472
ClinGenrs1057518472
ebirs1057518472
HLIrs1057518472
Exacrs1057518472
Gnomadrs1057518472
Varsomers1057518472
Maprs1057518472
PheGenIrs1057518472
Biobankrs1057518472
1000 genomesrs1057518472
hgdprs1057518472
ensemblrs1057518472
gopubmedrs1057518472
geneviewrs1057518472
scholarrs1057518472
googlers1057518472
pharmgkbrs1057518472
gwascentralrs1057518472
openSNPrs1057518472
23andMers1057518472
23andMe allrs1057518472
SNPshotrs1057518472
SNPdbers1057518472
MSV3drs1057518472
GWAS Ctlgrs1057518472
Max Magnitude0
ClinVar
Risk rs1057518472(C;C) rs1057518472(T;T)
Alt rs1057518472(C;C) rs1057518472(T;T)
Reference Rs1057518472(G;G)
Significance Probable-Pathogenic
Disease Familial adenomatous polyposis 1 not specified not provided
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 not specified not provided
Reversed 0
HGVS NC_000005.9:g.112174898G>C; NC_000005.9:g.112174898G>T
CLNSRC
CLNACC RCV000465493.1, RCV000479172.1, RCV000413595.1,