Have questions? Visit https://www.reddit.com/r/SNPedia

rs768922431

来自SNPedia
跳转至:导航搜索

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768922431(C;T)
Make rs768922431(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112842303
GeneAPC
is asnp
is mentioned by
dbSNPrs768922431
ebirs768922431
HLIrs768922431
Exacrs768922431
Varsomers768922431
Maprs768922431
PheGenIrs768922431
hapmaprs768922431
1000 genomesrs768922431
hgdprs768922431
ensemblrs768922431
gopubmedrs768922431
geneviewrs768922431
scholarrs768922431
googlers768922431
pharmgkbrs768922431
gwascentralrs768922431
openSNPrs768922431
23andMers768922431
23andMe allrs768922431
SNP Nexus

SNPshotrs768922431
SNPdbers768922431
MSV3drs768922431
GWAS Ctlgrs768922431
Max Magnitude0
ClinVar
Risk rs768922431(A,T;A,T)
Alt rs768922431(A,T;A,T)
Reference rs768922431(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome not provided
Variation info
Gene APC
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000005.9:g.112178000C>A; NC_000005.9:g.112178000C>T
CLNSRC
CLNACC RCV000219807.1, RCV000167356.1, RCV000237046.1,