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rs797044482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044482(-;T)
Make rs797044482(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position12718118
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs797044482
dbSNP (old)rs797044482
ClinGenrs797044482
ebirs797044482
HLIrs797044482
Exacrs797044482
Gnomadrs797044482
Varsomers797044482
Maprs797044482
PheGenIrs797044482
Biobankrs797044482
1000 genomesrs797044482
hgdprs797044482
ensemblrs797044482
gopubmedrs797044482
geneviewrs797044482
scholarrs797044482
googlers797044482
pharmgkbrs797044482
gwascentralrs797044482
openSNPrs797044482
23andMers797044482
23andMe allrs797044482
SNP Nexus

SNPshotrs797044482
SNPdbers797044482
MSV3drs797044482
GWAS Ctlgrs797044482
Max Magnitude0
ClinVar
Risk rs797044482(T;T)
Alt rs797044482(T;T)
Reference Rs797044482(-;-)
Significance Probable-Pathogenic
Disease Neuroendocrine neoplasm
Variation info
Gene LOC101929220 CDKN1B
CLNDBN Neuroendocrine neoplasm
Reversed 0
HGVS NC_000012.11:g.12871052_12871053insT
CLNSRC
CLNACC RCV000191952.1,