Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057521489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521489(G;T)
Make rs1057521489(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position9365464
GenePLCB4
is asnp
is mentioned by
dbSNPrs1057521489
dbSNP (old)rs1057521489
ClinGenrs1057521489
ebirs1057521489
HLIrs1057521489
Exacrs1057521489
Gnomadrs1057521489
Varsomers1057521489
Maprs1057521489
PheGenIrs1057521489
Biobankrs1057521489
1000 genomesrs1057521489
hgdprs1057521489
ensemblrs1057521489
gopubmedrs1057521489
geneviewrs1057521489
scholarrs1057521489
googlers1057521489
pharmgkbrs1057521489
gwascentralrs1057521489
openSNPrs1057521489
23andMers1057521489
23andMe allrs1057521489
SNPshotrs1057521489
SNPdbers1057521489
MSV3drs1057521489
GWAS Ctlgrs1057521489
Max Magnitude0
ClinVar
Risk rs1057521489(T;T)
Alt rs1057521489(T;T)
Reference Rs1057521489(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLCB4
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.9346111G>T
CLNSRC
CLNACC RCV000443167.1,