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

rs1057520630

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520630(A;A)
Make rs1057520630(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position49861607
GenePNKP
is asnp
is mentioned by
dbSNPrs1057520630
dbSNP (old)rs1057520630
ClinGenrs1057520630
ebirs1057520630
HLIrs1057520630
Exacrs1057520630
Gnomadrs1057520630
Varsomers1057520630
Maprs1057520630
PheGenIrs1057520630
Biobankrs1057520630
1000 genomesrs1057520630
hgdprs1057520630
ensemblrs1057520630
gopubmedrs1057520630
geneviewrs1057520630
scholarrs1057520630
googlers1057520630
pharmgkbrs1057520630
gwascentralrs1057520630
openSNPrs1057520630
23andMers1057520630
23andMe allrs1057520630
SNPshotrs1057520630
SNPdbers1057520630
MSV3drs1057520630
GWAS Ctlgrs1057520630
Max Magnitude0
ClinVar
Risk rs1057520630(A;A)
Alt rs1057520630(A;A)
Reference Rs1057520630(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.50364864C>T
CLNSRC
CLNACC RCV000423961.1,