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

rs151020551

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151020551(C;T)
Make rs151020551(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position46363699
GenePCNT
is asnp
is mentioned by
dbSNPrs151020551
ebirs151020551
HLIrs151020551
Exacrs151020551
Varsomers151020551
Maprs151020551
PheGenIrs151020551
hapmaprs151020551
1000 genomesrs151020551
hgdprs151020551
ensemblrs151020551
gopubmedrs151020551
geneviewrs151020551
scholarrs151020551
googlers151020551
pharmgkbrs151020551
gwascentralrs151020551
openSNPrs151020551
23andMers151020551
23andMe allrs151020551
SNP Nexus

SNPshotrs151020551
SNPdbers151020551
MSV3drs151020551
GWAS Ctlgrs151020551
Max Magnitude0
ClinVar
Risk rs151020551(T;T)
Alt rs151020551(T;T)
Reference rs151020551(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCNT
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.47783614C>T
CLNSRC
CLNACC RCV000171353.1,