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rs786203016

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203016(-;-)
Make rs786203016(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position57750968
GeneCDK4
is asnp
is mentioned by
dbSNPrs786203016
ebirs786203016
HLIrs786203016
Exacrs786203016
Varsomers786203016
Maprs786203016
PheGenIrs786203016
hapmaprs786203016
1000 genomesrs786203016
hgdprs786203016
ensemblrs786203016
gopubmedrs786203016
geneviewrs786203016
scholarrs786203016
googlers786203016
pharmgkbrs786203016
gwascentralrs786203016
openSNPrs786203016
23andMers786203016
23andMe allrs786203016
SNP Nexus

SNPshotrs786203016
SNPdbers786203016
MSV3drs786203016
GWAS Ctlgrs786203016
Max Magnitude0
ClinVar
Risk rs786203016(;)
Alt rs786203016(;)
Reference rs786203016(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDK4
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000012.11:g.58144751delA
CLNSRC
CLNACC RCV000166135.1,